Canonical Allele Identifier: CA2646776905

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539706-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539708_100539709del , CM000663.2:g.100539708_100539709del	GRCh38
NC_000001.10:g.101005264_101005265del , CM000663.1:g.101005264_101005265del	GRCh37
NC_000001.9:g.100777852_100777853del	NCBI36
NG_053134.1:g.6537_6538del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.742_743del MANE Select	ENSP00000314223.4:p.Pro248GlyfsTer?
ENST00000315033.4:c.742_743del	ENSP00000314223.4:p.Pro248GlyfsTer?
NM_022049.2:c.742_743del	NP_071332.2:p.Pro248GlyfsTer?
NM_022049.3:c.742_743del MANE Select	NP_071332.2:p.Pro248GlyfsTer?