Canonical Allele Identifier: CA2278679926

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809730T= , CM000679.2:g.81809730T=	GRCh38
NC_000017.10:g.79767606T= , CM000679.1:g.79767606T=	GRCh37
NG_016409.1:g.8557T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-52T= MANE Select	ENSP00000383558.3:n.61-52T=
ENST00000400723.7:c.61-52T=	ENSP00000383558.3:n.61-52T=
ENST00000570996.5:c.61-52T=	ENSP00000460976.1:n.61-52T=
ENST00000572185.1:n.356-52T=
ENST00000573428.1:c.61-52T=	ENSP00000458930.1:n.61-52T=
NM_000160.4:c.61-52T=	NP_000151.1:n.61-52T=
XM_006722277.1:c.61-52T=	XP_006722340.1:n.61-52T=
XM_011523539.1:c.-166-52T=	XP_011521841.1:n.-166-52T=
XM_011523540.1:c.-456-52T=	XP_011521842.1:n.-456-52T=
XM_017024446.1:c.61-58T=	XP_016879935.1:n.61-58T=
XM_017024447.1:c.-450-58T=	XP_016879936.1:n.-450-58T=
NM_000160.5:c.61-52T= MANE Select	NP_000151.1:n.61-52T=