Canonical Allele Identifier: CA2810641541

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809656_81809668del , CM000679.2:g.81809656_81809668del	GRCh38
NC_000017.10:g.79767532_79767544del , CM000679.1:g.79767532_79767544del	GRCh37
NG_016409.1:g.8483_8495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-126_61-114del MANE Select	ENSP00000383558.3:n.61-126_61-114del
ENST00000400723.7:c.61-126_61-114del	ENSP00000383558.3:n.61-126_61-114del
ENST00000570996.5:c.61-126_61-114del	ENSP00000460976.1:n.61-126_61-114del
ENST00000572185.1:n.356-126_356-114del
ENST00000573428.1:c.61-126_61-114del	ENSP00000458930.1:n.61-126_61-114del
NM_000160.4:c.61-126_61-114del	NP_000151.1:n.61-126_61-114del
XM_006722277.1:c.61-126_61-114del	XP_006722340.1:n.61-126_61-114del
XM_011523539.1:c.-166-126_-166-114del	XP_011521841.1:n.-166-126_-166-114del
XM_011523540.1:c.-456-126_-456-114del	XP_011521842.1:n.-456-126_-456-114del
XM_017024446.1:c.61-132_61-120del	XP_016879935.1:n.61-132_61-120del
XM_017024447.1:c.-450-132_-450-120del	XP_016879936.1:n.-450-132_-450-120del
NM_000160.5:c.61-126_61-114del MANE Select	NP_000151.1:n.61-126_61-114del