Canonical Allele Identifier: CA1174911545

Gene: NEGR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.71605449_71605453delinsCGGTA , CM000663.2:g.71605449_71605453delinsCGGTA	GRCh38
NC_000001.10:g.72071132_72071136delinsCGGTA , CM000663.1:g.72071132_72071136delinsCGGTA	GRCh37
NC_000001.9:g.71843720_71843724delinsCGGTA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357731.10:c.788+5573_788+5577delinsTACCG MANE Select	ENSP00000350364.4:n.788+5573_788+5577deli...
ENST00000306821.3:c.404+5573_404+5577delinsTACCG	ENSP00000305938.3:n.404+5573_404+5577deli...
ENST00000357731.9:c.788+5573_788+5577delinsTACCG	ENSP00000350364.4:n.788+5573_788+5577deli...
ENST00000434200.5:c.623+5573_623+5577delinsTACCG	ENSP00000413294.2:n.623+5573_623+5577deli...
NM_173808.2:c.788+5573_788+5577delinsTACCG	NP_776169.2:n.788+5573_788+5577delinsTACC...
XM_011541200.1:c.788+5573_788+5577delinsTACCG	XP_011539502.1:n.788+5573_788+5577delinsT...
XM_011541200.3:c.788+5573_788+5577delinsTACCG	XP_011539502.1:n.788+5573_788+5577delinsT...
NM_173808.3:c.788+5573_788+5577delinsTACCG MANE Select	NP_776169.2:n.788+5573_788+5577delinsTACC...