Canonical Allele Identifier: CA1184190993
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539689C= , CM000663.2:g.100539689C= GRCh38
NC_000001.10:g.101005245C= , CM000663.1:g.101005245C= GRCh37
NC_000001.9:g.100777833C= NCBI36
NG_053134.1:g.6518C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.723C= MANE Select ENSP00000314223.4:p.Ala241=
ENST00000315033.4:c.723C= ENSP00000314223.4:p.Ala241=
NM_022049.2:c.723C= NP_071332.2:p.Ala241=
NM_022049.3:c.723C= MANE Select NP_071332.2:p.Ala241=
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