Canonical Allele Identifier: CA346776707
Gene: NRXN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.50497348A>T , CM000664.2:g.50497348A>T GRCh38
NC_000002.11:g.50724486A>T , CM000664.1:g.50724486A>T GRCh37
NC_000002.10:g.50577990A>T NCBI36
NG_011878.1:g.540189T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401669.7:c.2864T>A MANE Select ENSP00000385017.2:p.Val955Asp
ENST00000462791.2:n.840T>A
ENST00000636298.1:n.1763T>A
ENST00000637889.1:n.31T>A
ENST00000331040.9:c.2018T>A ENSP00000489573.1:p.Val673Asp
ENST00000401669.6:c.2864T>A ENSP00000385017.2:p.Val955Asp
ENST00000402717.6:c.2009T>A ENSP00000385434.4:p.Val670Asp
ENST00000404971.5:c.2984T>A ENSP00000385142.1:p.Val995Asp
ENST00000405472.7:c.2828T>A ENSP00000434015.2:p.Val943Asp
ENST00000406316.6:c.2864T>A ENSP00000384311.2:p.Val955Asp
ENST00000406859.7:c.2054T>A ENSP00000385681.4:p.Val685Asp
ENST00000625672.2:c.2840T>A ENSP00000485887.1:p.Val947Asp
ENST00000630543.2:c.2840T>A ENSP00000486879.1:p.Val947Asp
NM_001135659.1:c.2984T>A NP_001129131.1:p.Val995Asp
NM_004801.4:c.2864T>A NP_004792.1:p.Val955Asp
XM_005264642.2:c.2885T>A XP_005264699.1:p.Val962Asp
XM_005264643.2:c.2840T>A XP_005264700.1:p.Val947Asp
XM_006712137.2:c.2885T>A XP_006712200.1:p.Val962Asp
XM_006712140.2:c.2885T>A XP_006712203.1:p.Val962Asp
XM_006712141.2:c.2885T>A XP_006712204.1:p.Val962Asp
XM_011533167.1:c.2885T>A XP_011531469.1:p.Val962Asp
XM_011533168.1:c.2882T>A XP_011531470.1:p.Val961Asp
XM_011533169.1:c.2873T>A XP_011531471.1:p.Val958Asp
XM_011533170.1:c.2867T>A XP_011531472.1:p.Val956Asp
XM_011533171.1:c.2864T>A XP_011531473.1:p.Val955Asp
XM_011533172.1:c.2858T>A XP_011531474.1:p.Val953Asp
XM_011533173.1:c.2855T>A XP_011531475.1:p.Val952Asp
XM_011533174.1:c.2840T>A XP_011531476.1:p.Val947Asp
XM_011533175.1:c.2828T>A XP_011531477.1:p.Val943Asp
XM_011533176.1:c.2825T>A XP_011531478.1:p.Val942Asp
XM_011533177.1:c.2885T>A XP_011531479.1:p.Val962Asp
XM_011533178.1:c.2795T>A XP_011531480.1:p.Val932Asp
XM_011533179.1:c.2840T>A XP_011531481.1:p.Val947Asp
XM_011533180.1:c.2885T>A XP_011531482.1:p.Val962Asp
XM_011533181.1:c.2090T>A XP_011531483.1:p.Val697Asp
XM_011533182.1:c.2045T>A XP_011531484.1:p.Val682Asp
XM_011533183.1:c.2018T>A XP_011531485.1:p.Val673Asp
XM_011533184.1:c.1925T>A XP_011531486.1:p.Val642Asp
NM_001135659.2:c.2984T>A NP_001129131.1:p.Val995Asp
NM_001330077.1:c.2840T>A NP_001317006.1:p.Val947Asp
NM_001330078.1:c.2864T>A NP_001317007.1:p.Val955Asp
NM_001330082.1:c.2840T>A NP_001317011.1:p.Val947Asp
NM_001330083.1:c.2798T>A NP_001317012.1:p.Val933Asp
NM_001330084.1:c.2798T>A NP_001317013.1:p.Val933Asp
NM_001330085.1:c.2837T>A NP_001317014.1:p.Val946Asp
NM_001330086.1:c.2864T>A NP_001317015.1:p.Val955Asp
NM_001330087.1:c.2753T>A NP_001317016.1:p.Val918Asp
NM_001330088.1:c.2783T>A NP_001317017.1:p.Val928Asp
NM_001330093.1:c.2861T>A NP_001317022.1:p.Val954Asp
NM_001330094.1:c.2852T>A NP_001317023.1:p.Val951Asp
NM_001330095.1:c.2813T>A NP_001317024.1:p.Val938Asp
NM_001330096.1:c.2753T>A NP_001317025.1:p.Val918Asp
NM_004801.5:c.2864T>A NP_004792.1:p.Val955Asp
XM_005264642.4:c.2885T>A XP_005264699.1:p.Val962Asp
XM_006712137.4:c.2885T>A XP_006712200.1:p.Val962Asp
XM_006712140.4:c.2885T>A XP_006712203.2:p.Val962Asp
XM_011533167.3:c.2885T>A XP_011531469.1:p.Val962Asp
XM_011533172.3:c.2858T>A XP_011531474.1:p.Val953Asp
XM_011533175.3:c.2828T>A XP_011531477.1:p.Val943Asp
XM_011533177.3:c.2885T>A XP_011531479.1:p.Val962Asp
XM_011533178.3:c.2795T>A XP_011531480.1:p.Val932Asp
XM_011533180.3:c.2885T>A XP_011531482.1:p.Val962Asp
XM_011533183.2:c.2018T>A XP_011531485.1:p.Val673Asp
XM_017005303.2:c.2885T>A XP_016860792.1:p.Val962Asp
XM_017005304.2:c.2882T>A XP_016860793.1:p.Val961Asp
XM_017005305.2:c.2885T>A XP_016860794.1:p.Val962Asp
XM_017005306.2:c.2873T>A XP_016860795.1:p.Val958Asp
XM_017005307.2:c.2867T>A XP_016860796.1:p.Val956Asp
XM_017005308.2:c.2864T>A XP_016860797.1:p.Val955Asp
XM_017005309.2:c.2858T>A XP_016860798.1:p.Val953Asp
XM_017005310.2:c.2855T>A XP_016860799.1:p.Val952Asp
XM_017005311.2:c.2840T>A XP_016860800.1:p.Val947Asp
XM_017005314.2:c.2825T>A XP_016860803.1:p.Val942Asp
XM_017005315.2:c.2858T>A XP_016860804.1:p.Val953Asp
XM_017005316.2:c.2822T>A XP_016860805.1:p.Val941Asp
XM_017005318.2:c.2813T>A XP_016860807.1:p.Val938Asp
XM_017005320.2:c.2837T>A XP_016860809.1:p.Val946Asp
XM_017005321.2:c.2885T>A XP_016860810.1:p.Val962Asp
XM_017005322.2:c.2885T>A XP_016860811.1:p.Val962Asp
XM_017005324.2:c.2858T>A XP_016860813.1:p.Val953Asp
XM_017005325.2:c.2858T>A XP_016860814.1:p.Val953Asp
XM_017005326.2:c.2846T>A XP_016860815.1:p.Val949Asp
XM_017005327.2:c.2840T>A XP_016860816.1:p.Val947Asp
XM_017005329.2:c.2885T>A XP_016860818.1:p.Val962Asp
XM_017005334.2:c.1925T>A XP_016860823.1:p.Val642Asp
NM_001330078.2:c.2864T>A MANE Select NP_001317007.1:p.Val955Asp
NM_001135659.3:c.2984T>A NP_001129131.1:p.Val995Asp
NM_001330077.2:c.2840T>A NP_001317006.1:p.Val947Asp
NM_001330082.2:c.2840T>A NP_001317011.1:p.Val947Asp
NM_001330083.2:c.2798T>A NP_001317012.1:p.Val933Asp
NM_001330084.2:c.2798T>A NP_001317013.1:p.Val933Asp
NM_001330085.2:c.2837T>A NP_001317014.1:p.Val946Asp
NM_001330086.2:c.2864T>A NP_001317015.1:p.Val955Asp
NM_001330087.2:c.2753T>A NP_001317016.1:p.Val918Asp
NM_001330088.2:c.2783T>A NP_001317017.1:p.Val928Asp
NM_001330093.2:c.2861T>A NP_001317022.1:p.Val954Asp
NM_001330094.2:c.2852T>A NP_001317023.1:p.Val951Asp
NM_001330095.2:c.2813T>A NP_001317024.1:p.Val938Asp
NM_001330096.2:c.2753T>A NP_001317025.1:p.Val918Asp
NM_004801.6:c.2864T>A NP_004792.1:p.Val955Asp