Canonical Allele Identifier: CA2696365036

Gene: NEGR1

Linked Data

• dbSNP Id: rs2101536327

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71605332T>A , CM000663.2:g.71605332T>A	GRCh38
NC_000001.10:g.72071015T>A , CM000663.1:g.72071015T>A	GRCh37
NC_000001.9:g.71843603T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357731.10:c.788+5694A>T MANE Select	ENSP00000350364.4:n.788+5694A>T
ENST00000306821.3:c.404+5694A>T	ENSP00000305938.3:n.404+5694A>T
ENST00000357731.9:c.788+5694A>T	ENSP00000350364.4:n.788+5694A>T
ENST00000434200.5:c.623+5694A>T	ENSP00000413294.2:n.623+5694A>T
NM_173808.2:c.788+5694A>T	NP_776169.2:n.788+5694A>T
XM_011541200.1:c.788+5694A>T	XP_011539502.1:n.788+5694A>T
XM_011541200.3:c.788+5694A>T	XP_011539502.1:n.788+5694A>T
NM_173808.3:c.788+5694A>T MANE Select	NP_776169.2:n.788+5694A>T