Canonical Allele Identifier: CA1184191007
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651710025

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539714_100539731dup , CM000663.2:g.100539714_100539731dup GRCh38
NC_000001.10:g.101005270_101005287dup , CM000663.1:g.101005270_101005287dup GRCh37
NC_000001.9:g.100777858_100777875dup NCBI36
NG_053134.1:g.6543_6560dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.748_765dup MANE Select ENSP00000314223.4:p.Gly255_Pro256insAlaGlnHisAlaProGly
ENST00000315033.4:c.748_765dup ENSP00000314223.4:p.Gly255_Pro256insAlaGlnHisAlaProGly
NM_022049.2:c.748_765dup NP_071332.2:p.Gly255_Pro256insAlaGlnHisAlaProGly
NM_022049.3:c.748_765dup MANE Select NP_071332.2:p.Gly255_Pro256insAlaGlnHisAlaProGly