Canonical Allele Identifier: CA2278680012

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809875C= , CM000679.2:g.81809875C=	GRCh38
NC_000017.10:g.79767751C= , CM000679.1:g.79767751C=	GRCh37
NG_016409.1:g.8702C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.154C= MANE Select	ENSP00000383558.3:p.Pro52=
ENST00000400723.7:c.154C=	ENSP00000383558.3:p.Pro52=
ENST00000570996.5:c.154C=	ENSP00000460976.1:p.Pro52=
ENST00000572185.1:n.449C=
ENST00000573428.1:c.154C=	ENSP00000458930.1:p.Pro52=
ENST00000574283.2:n.88C=
NM_000160.4:c.154C=	NP_000151.1:p.Pro52=
XM_006722277.1:c.154C=	XP_006722340.1:p.Pro52=
XM_011523539.1:c.-73C=	XP_011521841.1:n.-73C=
XM_011523540.1:c.-363C=	XP_011521842.1:n.-363C=
XM_017024446.1:c.148C=	XP_016879935.1:p.Pro50=
XM_017024447.1:c.-363C=	XP_016879936.1:n.-363C=
NM_000160.5:c.154C= MANE Select	NP_000151.1:p.Pro52=