Canonical Allele Identifier: CA2278680025

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809901G= , CM000679.2:g.81809901G=	GRCh38
NC_000017.10:g.79767777G= , CM000679.1:g.79767777G=	GRCh37
NG_016409.1:g.8728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+17G= MANE Select	ENSP00000383558.3:n.163+17G=
ENST00000400723.7:c.163+17G=	ENSP00000383558.3:n.163+17G=
ENST00000570996.5:c.163+17G=	ENSP00000460976.1:n.163+17G=
ENST00000572185.1:n.475G=
ENST00000573428.1:c.163+17G=	ENSP00000458930.1:n.163+17G=
ENST00000574283.2:n.114G=
NM_000160.4:c.163+17G=	NP_000151.1:n.163+17G=
XM_006722277.1:c.163+17G=	XP_006722340.1:n.163+17G=
XM_011523539.1:c.-47G=	XP_011521841.1:n.-47G=
XM_011523540.1:c.-337G=	XP_011521842.1:n.-337G=
XM_017024446.1:c.157+17G=	XP_016879935.1:n.157+17G=
XM_017024447.1:c.-337G=	XP_016879936.1:n.-337G=
NM_000160.5:c.163+17G= MANE Select	NP_000151.1:n.163+17G=