Canonical Allele Identifier: CA2278679842

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809646_81809650delinsCCTGT , CM000679.2:g.81809646_81809650delinsCCTGT	GRCh38
NC_000017.10:g.79767522_79767526delinsCCTGT , CM000679.1:g.79767522_79767526delinsCCTGT	GRCh37
NG_016409.1:g.8473_8477delinsCCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-136_61-132delinsCCTGT MANE Select	ENSP00000383558.3:n.61-136_61-132delinsCCTGT
ENST00000400723.7:c.61-136_61-132delinsCCTGT	ENSP00000383558.3:n.61-136_61-132delinsCCTGT
ENST00000570996.5:c.61-136_61-132delinsCCTGT	ENSP00000460976.1:n.61-136_61-132delinsCCTGT
ENST00000572185.1:n.356-136_356-132delinsCCTGT
ENST00000573428.1:c.61-136_61-132delinsCCTGT	ENSP00000458930.1:n.61-136_61-132delinsCCTGT
NM_000160.4:c.61-136_61-132delinsCCTGT	NP_000151.1:n.61-136_61-132delinsCCTGT
XM_006722277.1:c.61-136_61-132delinsCCTGT	XP_006722340.1:n.61-136_61-132delinsCCTGT
XM_011523539.1:c.-166-136_-166-132delinsCCTGT	XP_011521841.1:n.-166-136_-166-132delinsCCTGT
XM_011523540.1:c.-456-136_-456-132delinsCCTGT	XP_011521842.1:n.-456-136_-456-132delinsCCTGT
XM_017024446.1:c.61-142_61-138delinsCCTGT	XP_016879935.1:n.61-142_61-138delinsCCTGT
XM_017024447.1:c.-450-142_-450-138delinsCCTGT	XP_016879936.1:n.-450-142_-450-138delinsCCTGT
NM_000160.5:c.61-136_61-132delinsCCTGT MANE Select	NP_000151.1:n.61-136_61-132delinsCCTGT