Canonical Allele Identifier: CA2278680059

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809978T= , CM000679.2:g.81809978T=	GRCh38
NC_000017.10:g.79767854T= , CM000679.1:g.79767854T=	GRCh37
NG_016409.1:g.8805T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+94T= MANE Select	ENSP00000383558.3:n.163+94T=
ENST00000400723.7:c.163+94T=	ENSP00000383558.3:n.163+94T=
ENST00000570996.5:c.163+94T=	ENSP00000460976.1:n.163+94T=
ENST00000572185.1:n.552T=
ENST00000573428.1:c.163+94T=	ENSP00000458930.1:n.163+94T=
ENST00000574283.2:n.191T=
NM_000160.4:c.163+94T=	NP_000151.1:n.163+94T=
XM_006722277.1:c.163+94T=	XP_006722340.1:n.163+94T=
XM_011523539.1:c.31T=	XP_011521841.1:p.Phe11=
XM_011523540.1:c.-260T=	XP_011521842.1:n.-260T=
XM_017024446.1:c.157+94T=	XP_016879935.1:n.157+94T=
XM_017024447.1:c.-260T=	XP_016879936.1:n.-260T=
NM_000160.5:c.163+94T= MANE Select	NP_000151.1:n.163+94T=