Canonical Allele Identifier: CA1184191322
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539959C= , CM000663.2:g.100539959C= GRCh38
NC_000001.10:g.101005515C= , CM000663.1:g.101005515C= GRCh37
NC_000001.9:g.100778103C= NCBI36
NG_053134.1:g.6788C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.993C= MANE Select ENSP00000314223.4:p.Leu331=
ENST00000315033.4:c.993C= ENSP00000314223.4:p.Leu331=
NM_022049.2:c.993C= NP_071332.2:p.Leu331=
NM_022049.3:c.993C= MANE Select NP_071332.2:p.Leu331=
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