Canonical Allele Identifier: CA2744082839
Gene: NEGR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71605443A>T , CM000663.2:g.71605443A>T GRCh38
NC_000001.10:g.72071126A>T , CM000663.1:g.72071126A>T GRCh37
NC_000001.9:g.71843714A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357731.10:c.788+5583T>A MANE Select ENSP00000350364.4:n.788+5583T>A
ENST00000306821.3:c.404+5583T>A ENSP00000305938.3:n.404+5583T>A
ENST00000357731.9:c.788+5583T>A ENSP00000350364.4:n.788+5583T>A
ENST00000434200.5:c.623+5583T>A ENSP00000413294.2:n.623+5583T>A
NM_173808.2:c.788+5583T>A NP_776169.2:n.788+5583T>A
XM_011541200.1:c.788+5583T>A XP_011539502.1:n.788+5583T>A
XM_011541200.3:c.788+5583T>A XP_011539502.1:n.788+5583T>A
NM_173808.3:c.788+5583T>A MANE Select NP_776169.2:n.788+5583T>A
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