Canonical Allele Identifier: CA341393054

Gene: GPR88

Linked Data

• gnomAD v4: 1-100540033-A-C
• MyVariant Identifiers: chr1:g.101005589A>C (hg19) ; chr1:g.100540033A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100540033A>C , CM000663.2:g.100540033A>C	GRCh38
NC_000001.10:g.101005589A>C , CM000663.1:g.101005589A>C	GRCh37
NC_000001.9:g.100778177A>C	NCBI36
NG_053134.1:g.6862A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.1067A>C MANE Select	ENSP00000314223.4:p.Asp356Ala
ENST00000315033.4:c.1067A>C	ENSP00000314223.4:p.Asp356Ala
NM_022049.2:c.1067A>C	NP_071332.2:p.Asp356Ala
NM_022049.3:c.1067A>C MANE Select	NP_071332.2:p.Asp356Ala