Canonical Allele Identifier: CA10903392
Gene: NEGR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10493485

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.71605446A>T , CM000663.2:g.71605446A>T GRCh38
NC_000001.10:g.72071129A>T , CM000663.1:g.72071129A>T GRCh37
NC_000001.9:g.71843717A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_173808.2:c.788+5580T>A VV NP_776169.2:p.=
XM_011541200.1:c.788+5580T>A XP_011539502.1:p.=
XM_011541200.3:c.788+5580T>A XP_011539502.1:p.=
NM_173808.3:c.788+5580T>A VV MANE Preferred NP_776169.2:p.=
ENST00000306821.3:c.404+5580T>A ENSP00000305938.3:p.=
ENST00000357731.9:c.788+5580T>A ENSP00000350364.4:p.=
ENST00000434200.5:n.623+5580T>A ENSP00000413294.2:p.=