Canonical Allele Identifier: CA2278679823

Gene: GCGR

Linked Data

• dbSNP Id: rs2038049282

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809628_81809629insACCT , CM000679.2:g.81809628_81809629insACCT	GRCh38
NC_000017.10:g.79767504_79767505insACCT , CM000679.1:g.79767504_79767505insACCT	GRCh37
NG_016409.1:g.8455_8456insACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-154_61-153insACCT MANE Select	ENSP00000383558.3:n.61-154_61-153insACCT
ENST00000400723.7:c.61-154_61-153insACCT	ENSP00000383558.3:n.61-154_61-153insACCT
ENST00000570996.5:c.61-154_61-153insACCT	ENSP00000460976.1:n.61-154_61-153insACCT
ENST00000572185.1:n.356-154_356-153insACCT
ENST00000573428.1:c.61-154_61-153insACCT	ENSP00000458930.1:n.61-154_61-153insACCT
NM_000160.4:c.61-154_61-153insACCT	NP_000151.1:n.61-154_61-153insACCT
XM_006722277.1:c.61-154_61-153insACCT	XP_006722340.1:n.61-154_61-153insACCT
XM_011523539.1:c.-166-154_-166-153insACCT	XP_011521841.1:n.-166-154_-166-153insACCT
XM_011523540.1:c.-456-154_-456-153insACCT	XP_011521842.1:n.-456-154_-456-153insACCT
XM_017024446.1:c.61-160_61-159insACCT	XP_016879935.1:n.61-160_61-159insACCT
XM_017024447.1:c.-450-160_-450-159insACCT	XP_016879936.1:n.-450-160_-450-159insACCT
NM_000160.5:c.61-154_61-153insACCT MANE Select	NP_000151.1:n.61-154_61-153insACCT