Canonical Allele Identifier: CA401491272

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767716G>A (hg19) ; chr17:g.81809840G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809840G>A , CM000679.2:g.81809840G>A	GRCh38
NC_000017.10:g.79767716G>A , CM000679.1:g.79767716G>A	GRCh37
NG_016409.1:g.8667G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.119G>A MANE Select	ENSP00000383558.3:p.Gly40Asp
ENST00000400723.7:c.119G>A	ENSP00000383558.3:p.Gly40Asp
ENST00000570996.5:c.119G>A	ENSP00000460976.1:p.Gly40Asp
ENST00000572185.1:n.414G>A
ENST00000573428.1:c.119G>A	ENSP00000458930.1:p.Gly40Asp
ENST00000574283.2:n.53G>A
NM_000160.4:c.119G>A	NP_000151.1:p.Gly40Asp
XM_006722277.1:c.119G>A	XP_006722340.1:p.Gly40Asp
XM_011523539.1:c.-108G>A	XP_011521841.1:n.-108G>A
XM_011523540.1:c.-398G>A	XP_011521842.1:n.-398G>A
XM_017024446.1:c.113G>A	XP_016879935.1:p.Gly38Asp
XM_017024447.1:c.-398G>A	XP_016879936.1:n.-398G>A
NM_000160.5:c.119G>A MANE Select	NP_000151.1:p.Gly40Asp