Canonical Allele Identifier: CA401491332

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767722A>C (hg19) ; chr17:g.81809846A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809846A>C , CM000679.2:g.81809846A>C	GRCh38
NC_000017.10:g.79767722A>C , CM000679.1:g.79767722A>C	GRCh37
NG_016409.1:g.8673A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.125A>C MANE Select	ENSP00000383558.3:p.Gln42Pro
ENST00000400723.7:c.125A>C	ENSP00000383558.3:p.Gln42Pro
ENST00000570996.5:c.125A>C	ENSP00000460976.1:p.Gln42Pro
ENST00000572185.1:n.420A>C
ENST00000573428.1:c.125A>C	ENSP00000458930.1:p.Gln42Pro
ENST00000574283.2:n.59A>C
NM_000160.4:c.125A>C	NP_000151.1:p.Gln42Pro
XM_006722277.1:c.125A>C	XP_006722340.1:p.Gln42Pro
XM_011523539.1:c.-102A>C	XP_011521841.1:n.-102A>C
XM_011523540.1:c.-392A>C	XP_011521842.1:n.-392A>C
XM_017024446.1:c.119A>C	XP_016879935.1:p.Gln40Pro
XM_017024447.1:c.-392A>C	XP_016879936.1:n.-392A>C
NM_000160.5:c.125A>C MANE Select	NP_000151.1:p.Gln42Pro