Canonical Allele Identifier: CA2278679858

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809663_81809670delinsCTGCCTGT , CM000679.2:g.81809663_81809670delinsCTGCCTGT	GRCh38
NC_000017.10:g.79767539_79767546delinsCTGCCTGT , CM000679.1:g.79767539_79767546delinsCTGCCTGT	GRCh37
NG_016409.1:g.8490_8497delinsCTGCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-119_61-112delinsCTGCCTGT MANE Select	ENSP00000383558.3:n.61-119_61-112delinsCTGCCTGT
ENST00000400723.7:c.61-119_61-112delinsCTGCCTGT	ENSP00000383558.3:n.61-119_61-112delinsCTGCCTGT
ENST00000570996.5:c.61-119_61-112delinsCTGCCTGT	ENSP00000460976.1:n.61-119_61-112delinsCTGCCTGT
ENST00000572185.1:n.356-119_356-112delinsCTGCCTGT
ENST00000573428.1:c.61-119_61-112delinsCTGCCTGT	ENSP00000458930.1:n.61-119_61-112delinsCTGCCTGT
NM_000160.4:c.61-119_61-112delinsCTGCCTGT	NP_000151.1:n.61-119_61-112delinsCTGCCTGT
XM_006722277.1:c.61-119_61-112delinsCTGCCTGT	XP_006722340.1:n.61-119_61-112delinsCTGCCTGT
XM_011523539.1:c.-166-119_-166-112delinsCTGCCTGT	XP_011521841.1:n.-166-119_-166-112delinsCTGCCTGT
XM_011523540.1:c.-456-119_-456-112delinsCTGCCTGT	XP_011521842.1:n.-456-119_-456-112delinsCTGCCTGT
XM_017024446.1:c.61-125_61-118delinsCTGCCTGT	XP_016879935.1:n.61-125_61-118delinsCTGCCTGT
XM_017024447.1:c.-450-125_-450-118delinsCTGCCTGT	XP_016879936.1:n.-450-125_-450-118delinsCTGCCTGT
NM_000160.5:c.61-119_61-112delinsCTGCCTGT MANE Select	NP_000151.1:n.61-119_61-112delinsCTGCCTGT