Canonical Allele Identifier: CA1174911565

Gene: NEGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71605494A= , CM000663.2:g.71605494A=	GRCh38
NC_000001.10:g.72071177A= , CM000663.1:g.72071177A=	GRCh37
NC_000001.9:g.71843765A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357731.10:c.788+5532T= MANE Select	ENSP00000350364.4:n.788+5532T=
ENST00000306821.3:c.404+5532T=	ENSP00000305938.3:n.404+5532T=
ENST00000357731.9:c.788+5532T=	ENSP00000350364.4:n.788+5532T=
ENST00000434200.5:c.623+5532T=	ENSP00000413294.2:n.623+5532T=
NM_173808.2:c.788+5532T=	NP_776169.2:n.788+5532T=
XM_011541200.1:c.788+5532T=	XP_011539502.1:n.788+5532T=
XM_011541200.3:c.788+5532T=	XP_011539502.1:n.788+5532T=
NM_173808.3:c.788+5532T= MANE Select	NP_776169.2:n.788+5532T=