Canonical Allele Identifier: CA11250125
Gene: NRXN1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1356888

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.50288880T>C , CM000664.2:g.50288880T>C GRCh38
NC_000002.11:g.50516018T>C , CM000664.1:g.50516018T>C GRCh37
NC_000002.10:g.50369522T>C NCBI36
NG_011878.1:g.748657A>G

Transcript Alleles

HGVS Amino-acid change
NM_001135659.1:c.3485-51910A>G VV NP_001129131.1:p.=
NM_004801.4:c.3365-51910A>G VV NP_004792.1:p.=
NM_138735.2:c.260-51910A>G VV NP_620072.1:p.=
XM_005264642.2:c.3386-51910A>G XP_005264699.1:p.=
XM_005264643.2:c.3341-51910A>G XP_005264700.1:p.=
XM_006712137.2:c.3386-51910A>G XP_006712200.1:p.=
XM_006712140.2:c.3386-51910A>G XP_006712203.1:p.=
XM_006712141.2:c.3386-51910A>G XP_006712204.1:p.=
XM_011533167.1:c.3386-51910A>G XP_011531469.1:p.=
XM_011533168.1:c.3383-51910A>G XP_011531470.1:p.=
XM_011533169.1:c.3374-51910A>G XP_011531471.1:p.=
XM_011533170.1:c.3368-51910A>G XP_011531472.1:p.=
XM_011533171.1:c.3365-51910A>G XP_011531473.1:p.=
XM_011533172.1:c.3359-51910A>G XP_011531474.1:p.=
XM_011533173.1:c.3356-51910A>G XP_011531475.1:p.=
XM_011533174.1:c.3341-51910A>G XP_011531476.1:p.=
XM_011533175.1:c.3329-51910A>G XP_011531477.1:p.=
XM_011533176.1:c.3326-51910A>G XP_011531478.1:p.=
XM_011533177.1:c.3386-51910A>G XP_011531479.1:p.=
XM_011533178.1:c.3296-51910A>G XP_011531480.1:p.=
XM_011533179.1:c.3341-51910A>G XP_011531481.1:p.=
XM_011533180.1:c.3386-51910A>G XP_011531482.1:p.=
XM_011533181.1:c.2591-51910A>G XP_011531483.1:p.=
XM_011533182.1:c.2546-51910A>G XP_011531484.1:p.=
XM_011533183.1:c.2519-51910A>G XP_011531485.1:p.=
XM_011533184.1:c.2426-51910A>G XP_011531486.1:p.=
NM_001135659.2:c.3485-51910A>G VV NP_001129131.1:p.=
NM_001330077.1:c.3341-51910A>G VV NP_001317006.1:p.=
NM_001330078.1:c.3365-51910A>G VV NP_001317007.1:p.=
NM_001330082.1:c.3341-51910A>G VV NP_001317011.1:p.=
NM_001330083.1:c.3299-51910A>G VV NP_001317012.1:p.=
NM_001330084.1:c.3299-51910A>G VV NP_001317013.1:p.=
NM_001330085.1:c.3338-51910A>G VV NP_001317014.1:p.=
NM_001330086.1:c.3365-51910A>G VV NP_001317015.1:p.=
NM_001330087.1:c.3254-51910A>G VV NP_001317016.1:p.=
NM_001330088.1:c.3284-51910A>G VV NP_001317017.1:p.=
NM_001330091.1:c.260-51910A>G VV NP_001317020.1:p.=
NM_001330092.1:c.260-51910A>G VV NP_001317021.1:p.=
NM_001330093.1:c.3362-51910A>G VV NP_001317022.1:p.=
NM_001330094.1:c.3353-51910A>G VV NP_001317023.1:p.=
NM_001330095.1:c.3314-51910A>G VV NP_001317024.1:p.=
NM_001330096.1:c.3254-51910A>G VV NP_001317025.1:p.=
NM_001330097.1:c.260-51910A>G VV NP_001317026.1:p.=
NM_004801.5:c.3365-51910A>G VV NP_004792.1:p.=
NM_138735.4:c.260-51910A>G VV NP_620072.1:p.=
XM_005264642.4:c.3386-51910A>G XP_005264699.1:p.=
XM_006712137.4:c.3386-51910A>G XP_006712200.1:p.=
XM_006712140.4:c.3413-51910A>G XP_006712203.2:p.=
XM_011533167.3:c.3386-51910A>G XP_011531469.1:p.=
XM_011533172.3:c.3359-51910A>G XP_011531474.1:p.=
XM_011533175.3:c.3329-51910A>G XP_011531477.1:p.=
XM_011533177.3:c.3386-51910A>G XP_011531479.1:p.=
XM_011533178.3:c.3296-51910A>G XP_011531480.1:p.=
XM_011533180.3:c.3386-51910A>G XP_011531482.1:p.=
XM_011533183.2:c.2519-51910A>G XP_011531485.1:p.=
XM_017005303.2:c.3413-51910A>G XP_016860792.1:p.=
XM_017005304.2:c.3410-51910A>G XP_016860793.1:p.=
XM_017005305.2:c.3413-51910A>G XP_016860794.1:p.=
XM_017005306.2:c.3401-51910A>G XP_016860795.1:p.=
XM_017005307.2:c.3395-51910A>G XP_016860796.1:p.=
XM_017005308.2:c.3392-51910A>G XP_016860797.1:p.=
XM_017005309.2:c.3386-51910A>G XP_016860798.1:p.=
XM_017005310.2:c.3383-51910A>G XP_016860799.1:p.=
XM_017005311.2:c.3368-51910A>G XP_016860800.1:p.=
XM_017005314.2:c.3353-51910A>G XP_016860803.1:p.=
XM_017005315.2:c.3359-51910A>G XP_016860804.1:p.=
XM_017005316.2:c.3350-51910A>G XP_016860805.1:p.=
XM_017005318.2:c.3341-51910A>G XP_016860807.1:p.=
XM_017005320.2:c.3338-51910A>G XP_016860809.1:p.=
XM_017005321.2:c.3413-51910A>G XP_016860810.1:p.=
XM_017005322.2:c.3413-51910A>G XP_016860811.1:p.=
XM_017005324.2:c.3359-51910A>G XP_016860813.1:p.=
XM_017005325.2:c.3359-51910A>G XP_016860814.1:p.=
XM_017005326.2:c.3347-51910A>G XP_016860815.1:p.=
XM_017005327.2:c.3341-51910A>G XP_016860816.1:p.=
XM_017005329.2:c.3413-51910A>G XP_016860818.1:p.=
XM_017005334.2:c.2453-51910A>G XP_016860823.1:p.=
NM_001330078.2:c.3365-51910A>G VV MANE Preferred NP_001317007.1:p.=
ENST00000331040.9:c.2519-51910A>G ENSP00000489573.1:p.=
ENST00000342183.9:c.260-51910A>G ENSP00000341184.5:p.=
ENST00000401669.6:c.3365-51910A>G ENSP00000385017.2:p.=
ENST00000401710.5:c.260-51910A>G ENSP00000385580.2:p.=
ENST00000404971.5:c.3485-51910A>G ENSP00000385142.1:p.=
ENST00000405472.7:c.3329-51910A>G ENSP00000434015.2:p.=
ENST00000406316.6:c.3365-51910A>G ENSP00000384311.2:p.=
ENST00000611589.4:c.-473-51910A>G ENSP00000483634.1:p.=
ENST00000625320.2:n.494-51910A>G ENSP00000486253.1:p.=
ENST00000625672.2:c.3341-51910A>G ENSP00000485887.1:p.=
ENST00000628364.2:c.260-51910A>G ENSP00000485815.1:p.=
ENST00000630543.2:n.3341-51910A>G ENSP00000486879.1:p.=
ENST00000635264.1:n.174-51910A>G