Canonical Allele Identifier: CA2278679835

Gene: GCGR

Linked Data

• dbSNP Id: rs2038049836

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809641_81809642insCCTG , CM000679.2:g.81809641_81809642insCCTG	GRCh38
NC_000017.10:g.79767517_79767518insCCTG , CM000679.1:g.79767517_79767518insCCTG	GRCh37
NG_016409.1:g.8468_8469insCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-141_61-140insCCTG MANE Select	ENSP00000383558.3:n.61-141_61-140insCCTG
ENST00000400723.7:c.61-141_61-140insCCTG	ENSP00000383558.3:n.61-141_61-140insCCTG
ENST00000570996.5:c.61-141_61-140insCCTG	ENSP00000460976.1:n.61-141_61-140insCCTG
ENST00000572185.1:n.356-141_356-140insCCTG
ENST00000573428.1:c.61-141_61-140insCCTG	ENSP00000458930.1:n.61-141_61-140insCCTG
NM_000160.4:c.61-141_61-140insCCTG	NP_000151.1:n.61-141_61-140insCCTG
XM_006722277.1:c.61-141_61-140insCCTG	XP_006722340.1:n.61-141_61-140insCCTG
XM_011523539.1:c.-166-141_-166-140insCCTG	XP_011521841.1:n.-166-141_-166-140insCCTG
XM_011523540.1:c.-456-141_-456-140insCCTG	XP_011521842.1:n.-456-141_-456-140insCCTG
XM_017024446.1:c.61-147_61-146insCCTG	XP_016879935.1:n.61-147_61-146insCCTG
XM_017024447.1:c.-450-147_-450-146insCCTG	XP_016879936.1:n.-450-147_-450-146insCCTG
NM_000160.5:c.61-141_61-140insCCTG MANE Select	NP_000151.1:n.61-141_61-140insCCTG