Canonical Allele Identifier: CA1184191400
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540022G= , CM000663.2:g.100540022G= GRCh38
NC_000001.10:g.101005578G= , CM000663.1:g.101005578G= GRCh37
NC_000001.9:g.100778166G= NCBI36
NG_053134.1:g.6851G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1056G= MANE Select ENSP00000314223.4:p.Pro352=
ENST00000315033.4:c.1056G= ENSP00000314223.4:p.Pro352=
NM_022049.2:c.1056G= NP_071332.2:p.Pro352=
NM_022049.3:c.1056G= MANE Select NP_071332.2:p.Pro352=
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