Canonical Allele Identifier: CA738477460

Gene: NEGR1

Linked Data

• dbSNP Id: rs1206987386
• gnomAD v3: 1-71605300-T-A
• gnomAD v4: 1-71605300-T-A
• MyVariant Identifiers: chr1:g.72070983T>A (hg19) ; chr1:g.71605300T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71605300T>A , CM000663.2:g.71605300T>A	GRCh38
NC_000001.10:g.72070983T>A , CM000663.1:g.72070983T>A	GRCh37
NC_000001.9:g.71843571T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357731.10:c.788+5726A>T MANE Select	ENSP00000350364.4:n.788+5726A>T
ENST00000306821.3:c.404+5726A>T	ENSP00000305938.3:n.404+5726A>T
ENST00000357731.9:c.788+5726A>T	ENSP00000350364.4:n.788+5726A>T
ENST00000434200.5:c.623+5726A>T	ENSP00000413294.2:n.623+5726A>T
NM_173808.2:c.788+5726A>T	NP_776169.2:n.788+5726A>T
XM_011541200.1:c.788+5726A>T	XP_011539502.1:n.788+5726A>T
XM_011541200.3:c.788+5726A>T	XP_011539502.1:n.788+5726A>T
NM_173808.3:c.788+5726A>T MANE Select	NP_776169.2:n.788+5726A>T