Canonical Allele Identifier: CA1184191482

Gene: GPR88

Linked Data

• dbSNP Id: rs1651726977

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100540066del , CM000663.2:g.100540066del	GRCh38
NC_000001.10:g.101005622del , CM000663.1:g.101005622del	GRCh37
NC_000001.9:g.100778210del	NCBI36
NG_053134.1:g.6895del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.1100del MANE Select	ENSP00000314223.4:p.Val367GlyfsTer?
ENST00000315033.4:c.1100del	ENSP00000314223.4:p.Val367GlyfsTer?
NM_022049.2:c.1100del	NP_071332.2:p.Val367GlyfsTer?
NM_022049.3:c.1100del MANE Select	NP_071332.2:p.Val367GlyfsTer?