Canonical Allele Identifier: CA1184191403
Gene: GPR88 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540025C= , CM000663.2:g.100540025C= GRCh38
NC_000001.10:g.101005581C= , CM000663.1:g.101005581C= GRCh37
NC_000001.9:g.100778169C= NCBI36
NG_053134.1:g.6854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1059C= MANE Select ENSP00000314223.4:p.Gly353=
ENST00000315033.4:c.1059C= ENSP00000314223.4:p.Gly353=
NM_022049.2:c.1059C= NP_071332.2:p.Gly353=
NM_022049.3:c.1059C= MANE Select NP_071332.2:p.Gly353=