Canonical Allele Identifier: CA346819113

Gene: NRXN1

Linked Data

• MyVariant Identifiers: chr2:g.50318542G>C (hg19) ; chr2:g.50091404G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.50091404G>C , CM000664.2:g.50091404G>C	GRCh38
NC_000002.11:g.50318542G>C , CM000664.1:g.50318542G>C	GRCh37
NC_000002.10:g.50172046G>C	NCBI36
NG_011878.1:g.946133C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401669.7:c.3637C>G MANE Select	ENSP00000385017.2:p.His1213Asp
ENST00000637889.1:n.804C>G
ENST00000637906.1:c.524C>G	ENSP00000490198.1:n.524C>G
ENST00000342183.9:c.532C>G	ENSP00000341184.5:p.His178Asp
ENST00000401669.6:c.3637C>G	ENSP00000385017.2:p.His1213Asp
ENST00000401710.5:c.532C>G	ENSP00000385580.2:p.His178Asp
ENST00000404971.5:c.3757C>G	ENSP00000385142.1:p.His1253Asp
ENST00000405472.7:c.3601C>G	ENSP00000434015.2:p.His1201Asp
ENST00000406316.6:c.3637C>G	ENSP00000384311.2:p.His1213Asp
ENST00000611589.4:c.-201C>G	ENSP00000483634.1:n.-201C>G
ENST00000625672.2:c.3613C>G	ENSP00000485887.1:p.His1205Asp
ENST00000628364.2:c.532C>G	ENSP00000485815.1:p.His178Asp
ENST00000630543.2:c.3613C>G	ENSP00000486879.1:p.His1205Asp
ENST00000635264.1:n.446C>G
NM_001135659.1:c.3757C>G	NP_001129131.1:p.His1253Asp
NM_004801.4:c.3637C>G	NP_004792.1:p.His1213Asp
NM_138735.2:c.532C>G	NP_620072.1:p.His178Asp
XM_005264642.2:c.3658C>G	XP_005264699.1:p.His1220Asp
XM_005264643.2:c.3613C>G	XP_005264700.1:p.His1205Asp
XM_006712137.2:c.3658C>G	XP_006712200.1:p.His1220Asp
XM_006712140.2:c.3658C>G	XP_006712203.1:p.His1220Asp
XM_006712141.2:c.3658C>G	XP_006712204.1:p.His1220Asp
XM_011533167.1:c.3658C>G	XP_011531469.1:p.His1220Asp
XM_011533168.1:c.3655C>G	XP_011531470.1:p.His1219Asp
XM_011533169.1:c.3646C>G	XP_011531471.1:p.His1216Asp
XM_011533170.1:c.3640C>G	XP_011531472.1:p.His1214Asp
XM_011533171.1:c.3637C>G	XP_011531473.1:p.His1213Asp
XM_011533172.1:c.3631C>G	XP_011531474.1:p.His1211Asp
XM_011533173.1:c.3628C>G	XP_011531475.1:p.His1210Asp
XM_011533174.1:c.3613C>G	XP_011531476.1:p.His1205Asp
XM_011533175.1:c.3601C>G	XP_011531477.1:p.His1201Asp
XM_011533176.1:c.3598C>G	XP_011531478.1:p.His1200Asp
XM_011533177.1:c.3658C>G	XP_011531479.1:p.His1220Asp
XM_011533178.1:c.3568C>G	XP_011531480.1:p.His1190Asp
XM_011533179.1:c.3613C>G	XP_011531481.1:p.His1205Asp
XM_011533180.1:c.3658C>G	XP_011531482.1:p.His1220Asp
XM_011533181.1:c.2863C>G	XP_011531483.1:p.His955Asp
XM_011533182.1:c.2818C>G	XP_011531484.1:p.His940Asp
XM_011533183.1:c.2791C>G	XP_011531485.1:p.His931Asp
XM_011533184.1:c.2698C>G	XP_011531486.1:p.His900Asp
NM_001135659.2:c.3757C>G	NP_001129131.1:p.His1253Asp
NM_001330077.1:c.3613C>G	NP_001317006.1:p.His1205Asp
NM_001330078.1:c.3637C>G	NP_001317007.1:p.His1213Asp
NM_001330082.1:c.3613C>G	NP_001317011.1:p.His1205Asp
NM_001330083.1:c.3571C>G	NP_001317012.1:p.His1191Asp
NM_001330084.1:c.3571C>G	NP_001317013.1:p.His1191Asp
NM_001330085.1:c.3610C>G	NP_001317014.1:p.His1204Asp
NM_001330086.1:c.3637C>G	NP_001317015.1:p.His1213Asp
NM_001330087.1:c.3526C>G	NP_001317016.1:p.His1176Asp
NM_001330088.1:c.3556C>G	NP_001317017.1:p.His1186Asp
NM_001330091.1:c.532C>G	NP_001317020.1:p.His178Asp
NM_001330092.1:c.532C>G	NP_001317021.1:p.His178Asp
NM_001330093.1:c.3634C>G	NP_001317022.1:p.His1212Asp
NM_001330094.1:c.3625C>G	NP_001317023.1:p.His1209Asp
NM_001330095.1:c.3586C>G	NP_001317024.1:p.His1196Asp
NM_001330096.1:c.3526C>G	NP_001317025.1:p.His1176Asp
NM_001330097.1:c.532C>G	NP_001317026.1:p.His178Asp
NM_004801.5:c.3637C>G	NP_004792.1:p.His1213Asp
NM_138735.4:c.532C>G	NP_620072.1:p.His178Asp
XM_005264642.4:c.3658C>G	XP_005264699.1:p.His1220Asp
XM_006712137.4:c.3658C>G	XP_006712200.1:p.His1220Asp
XM_006712140.4:c.3685C>G	XP_006712203.2:p.His1229Asp
XM_011533167.3:c.3658C>G	XP_011531469.1:p.His1220Asp
XM_011533172.3:c.3631C>G	XP_011531474.1:p.His1211Asp
XM_011533175.3:c.3601C>G	XP_011531477.1:p.His1201Asp
XM_011533177.3:c.3658C>G	XP_011531479.1:p.His1220Asp
XM_011533178.3:c.3568C>G	XP_011531480.1:p.His1190Asp
XM_011533180.3:c.3658C>G	XP_011531482.1:p.His1220Asp
XM_011533183.2:c.2791C>G	XP_011531485.1:p.His931Asp
XM_017005303.2:c.3685C>G	XP_016860792.1:p.His1229Asp
XM_017005304.2:c.3682C>G	XP_016860793.1:p.His1228Asp
XM_017005305.2:c.3685C>G	XP_016860794.1:p.His1229Asp
XM_017005306.2:c.3673C>G	XP_016860795.1:p.His1225Asp
XM_017005307.2:c.3667C>G	XP_016860796.1:p.His1223Asp
XM_017005308.2:c.3664C>G	XP_016860797.1:p.His1222Asp
XM_017005309.2:c.3658C>G	XP_016860798.1:p.His1220Asp
XM_017005310.2:c.3655C>G	XP_016860799.1:p.His1219Asp
XM_017005311.2:c.3640C>G	XP_016860800.1:p.His1214Asp
XM_017005314.2:c.3625C>G	XP_016860803.1:p.His1209Asp
XM_017005315.2:c.3631C>G	XP_016860804.1:p.His1211Asp
XM_017005316.2:c.3622C>G	XP_016860805.1:p.His1208Asp
XM_017005318.2:c.3613C>G	XP_016860807.1:p.His1205Asp
XM_017005320.2:c.3610C>G	XP_016860809.1:p.His1204Asp
XM_017005321.2:c.3685C>G	XP_016860810.1:p.His1229Asp
XM_017005322.2:c.3685C>G	XP_016860811.1:p.His1229Asp
XM_017005324.2:c.3631C>G	XP_016860813.1:p.His1211Asp
XM_017005325.2:c.3631C>G	XP_016860814.1:p.His1211Asp
XM_017005326.2:c.3619C>G	XP_016860815.1:p.His1207Asp
XM_017005327.2:c.3613C>G	XP_016860816.1:p.His1205Asp
XM_017005329.2:c.3685C>G	XP_016860818.1:p.His1229Asp
XM_017005334.2:c.2725C>G	XP_016860823.1:p.His909Asp
NM_001330078.2:c.3637C>G MANE Select	NP_001317007.1:p.His1213Asp
NM_001135659.3:c.3757C>G	NP_001129131.1:p.His1253Asp
NM_001330077.2:c.3613C>G	NP_001317006.1:p.His1205Asp
NM_001330082.2:c.3613C>G	NP_001317011.1:p.His1205Asp
NM_001330083.2:c.3571C>G	NP_001317012.1:p.His1191Asp
NM_001330084.2:c.3571C>G	NP_001317013.1:p.His1191Asp
NM_001330085.2:c.3610C>G	NP_001317014.1:p.His1204Asp
NM_001330086.2:c.3637C>G	NP_001317015.1:p.His1213Asp
NM_001330087.2:c.3526C>G	NP_001317016.1:p.His1176Asp
NM_001330088.2:c.3556C>G	NP_001317017.1:p.His1186Asp
NM_001330091.2:c.532C>G	NP_001317020.1:p.His178Asp
NM_001330092.2:c.532C>G	NP_001317021.1:p.His178Asp
NM_001330093.2:c.3634C>G	NP_001317022.1:p.His1212Asp
NM_001330094.2:c.3625C>G	NP_001317023.1:p.His1209Asp
NM_001330095.2:c.3586C>G	NP_001317024.1:p.His1196Asp
NM_001330096.2:c.3526C>G	NP_001317025.1:p.His1176Asp
NM_001330097.2:c.532C>G	NP_001317026.1:p.His178Asp
NM_004801.6:c.3637C>G	NP_004792.1:p.His1213Asp
NM_138735.5:c.532C>G	NP_620072.1:p.His178Asp