Canonical Allele Identifier: CA341393031
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540020C>G , CM000663.2:g.100540020C>G GRCh38
NC_000001.10:g.101005576C>G , CM000663.1:g.101005576C>G GRCh37
NC_000001.9:g.100778164C>G NCBI36
NG_053134.1:g.6849C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1054C>G MANE Select ENSP00000314223.4:p.Pro352Ala
ENST00000315033.4:c.1054C>G ENSP00000314223.4:p.Pro352Ala
NM_022049.2:c.1054C>G NP_071332.2:p.Pro352Ala
NM_022049.3:c.1054C>G MANE Select NP_071332.2:p.Pro352Ala