Canonical Allele Identifier: CA2278679913

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809722_81809742delinsCCTGTCTGTCTGCCTGCCTGT , CM000679.2:g.81809722_81809742delinsCCTGTCTGTCTGCCTGCCTGT	GRCh38
NC_000017.10:g.79767598_79767618delinsCCTGTCTGTCTGCCTGCCTGT , CM000679.1:g.79767598_79767618delinsCCTGTCTGTCTGCCTGCCTGT	GRCh37
NG_016409.1:g.8549_8569delinsCCTGTCTGTCTGCCTGCCTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT MANE Select	ENSP00000383558.3:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
ENST00000400723.7:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT	ENSP00000383558.3:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
ENST00000570996.5:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT	ENSP00000460976.1:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
ENST00000572185.1:n.356-60_356-40delinsCCTGTCTGTCTGCCTGCCTGT
ENST00000573428.1:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT	ENSP00000458930.1:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
NM_000160.4:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT	NP_000151.1:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
XM_006722277.1:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT	XP_006722340.1:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT
XM_011523539.1:c.-166-60_-166-40delinsCCTGTCTGTCTGCCTGCCTGT	XP_011521841.1:n.-166-60_-166-40delinsCCTGTCTGTCTGCCTGCCTGT
XM_011523540.1:c.-456-60_-456-40delinsCCTGTCTGTCTGCCTGCCTGT	XP_011521842.1:n.-456-60_-456-40delinsCCTGTCTGTCTGCCTGCCTGT
XM_017024446.1:c.61-66_61-46delinsCCTGTCTGTCTGCCTGCCTGT	XP_016879935.1:n.61-66_61-46delinsCCTGTCTGTCTGCCTGCCTGT
XM_017024447.1:c.-450-66_-450-46delinsCCTGTCTGTCTGCCTGCCTGT	XP_016879936.1:n.-450-66_-450-46delinsCCTGTCTGTCTGCCTGCCTGT
NM_000160.5:c.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT MANE Select	NP_000151.1:n.61-60_61-40delinsCCTGTCTGTCTGCCTGCCTGT