Canonical Allele Identifier: CA2278679943

Gene: GCGR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809741_81809742delinsGT , CM000679.2:g.81809741_81809742delinsGT	GRCh38
NC_000017.10:g.79767617_79767618delinsGT , CM000679.1:g.79767617_79767618delinsGT	GRCh37
NG_016409.1:g.8568_8569delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.61-41_61-40delinsGT MANE Select	ENSP00000383558.3:n.61-41_61-40delinsGT
ENST00000400723.7:c.61-41_61-40delinsGT	ENSP00000383558.3:n.61-41_61-40delinsGT
ENST00000570996.5:c.61-41_61-40delinsGT	ENSP00000460976.1:n.61-41_61-40delinsGT
ENST00000572185.1:n.356-41_356-40delinsGT
ENST00000573428.1:c.61-41_61-40delinsGT	ENSP00000458930.1:n.61-41_61-40delinsGT
NM_000160.4:c.61-41_61-40delinsGT	NP_000151.1:n.61-41_61-40delinsGT
XM_006722277.1:c.61-41_61-40delinsGT	XP_006722340.1:n.61-41_61-40delinsGT
XM_011523539.1:c.-166-41_-166-40delinsGT	XP_011521841.1:n.-166-41_-166-40delinsGT
XM_011523540.1:c.-456-41_-456-40delinsGT	XP_011521842.1:n.-456-41_-456-40delinsGT
XM_017024446.1:c.61-47_61-46delinsGT	XP_016879935.1:n.61-47_61-46delinsGT
XM_017024447.1:c.-450-47_-450-46delinsGT	XP_016879936.1:n.-450-47_-450-46delinsGT
NM_000160.5:c.61-41_61-40delinsGT MANE Select	NP_000151.1:n.61-41_61-40delinsGT