Canonical Allele Identifier: CA2278679862

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809666_81809670delinsCCTGT , CM000679.2:g.81809666_81809670delinsCCTGT	GRCh38
NC_000017.10:g.79767542_79767546delinsCCTGT , CM000679.1:g.79767542_79767546delinsCCTGT	GRCh37
NG_016409.1:g.8493_8497delinsCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-116_61-112delinsCCTGT MANE Select	ENSP00000383558.3:n.61-116_61-112delinsCCTGT
ENST00000400723.7:c.61-116_61-112delinsCCTGT	ENSP00000383558.3:n.61-116_61-112delinsCCTGT
ENST00000570996.5:c.61-116_61-112delinsCCTGT	ENSP00000460976.1:n.61-116_61-112delinsCCTGT
ENST00000572185.1:n.356-116_356-112delinsCCTGT
ENST00000573428.1:c.61-116_61-112delinsCCTGT	ENSP00000458930.1:n.61-116_61-112delinsCCTGT
NM_000160.4:c.61-116_61-112delinsCCTGT	NP_000151.1:n.61-116_61-112delinsCCTGT
XM_006722277.1:c.61-116_61-112delinsCCTGT	XP_006722340.1:n.61-116_61-112delinsCCTGT
XM_011523539.1:c.-166-116_-166-112delinsCCTGT	XP_011521841.1:n.-166-116_-166-112delinsCCTGT
XM_011523540.1:c.-456-116_-456-112delinsCCTGT	XP_011521842.1:n.-456-116_-456-112delinsCCTGT
XM_017024446.1:c.61-122_61-118delinsCCTGT	XP_016879935.1:n.61-122_61-118delinsCCTGT
XM_017024447.1:c.-450-122_-450-118delinsCCTGT	XP_016879936.1:n.-450-122_-450-118delinsCCTGT
NM_000160.5:c.61-116_61-112delinsCCTGT MANE Select	NP_000151.1:n.61-116_61-112delinsCCTGT