Canonical Allele Identifier: CA913046935
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005440_101005441insCGCGTGGCGAACGTGGTG (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539884_100539885insCGCGTGGCGAACGTGGTG , CM000663.2:g.100539884_100539885insCGCGTGGCGAACGTGGTG GRCh38
NC_000001.10:g.101005440_101005441insCGCGTGGCGAACGTGGTG , CM000663.1:g.101005440_101005441insCGCGTGGCGAACGTGGTG GRCh37
NC_000001.9:g.100778028_100778029insCGCGTGGCGAACGTGGTG NCBI36
NG_053134.1:g.6713_6714insCGCGTGGCGAACGTGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.918_919insCGCGTGGCGAACGTGGTG MANE Select ENSP00000314223.4:p.Ala306_Ser307insArgValAlaAsnValVal
ENST00000315033.4:c.918_919insCGCGTGGCGAACGTGGTG ENSP00000314223.4:p.Ala306_Ser307insArgValAlaAsnValVal
NM_022049.2:c.918_919insCGCGTGGCGAACGTGGTG NP_071332.2:p.Ala306_Ser307insArgValAlaAsnValVal
NM_022049.3:c.918_919insCGCGTGGCGAACGTGGTG MANE Select NP_071332.2:p.Ala306_Ser307insArgValAlaAsnValVal
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