Canonical Allele Identifier: CA2640508826

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809722-C-CCTGA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809725_81809726insACTG , CM000679.2:g.81809725_81809726insACTG	GRCh38
NC_000017.10:g.79767601_79767602insACTG , CM000679.1:g.79767601_79767602insACTG	GRCh37
NG_016409.1:g.8552_8553insACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-57_61-56insACTG MANE Select	ENSP00000383558.3:n.61-57_61-56insACTG
ENST00000400723.7:c.61-57_61-56insACTG	ENSP00000383558.3:n.61-57_61-56insACTG
ENST00000570996.5:c.61-57_61-56insACTG	ENSP00000460976.1:n.61-57_61-56insACTG
ENST00000572185.1:n.356-57_356-56insACTG
ENST00000573428.1:c.61-57_61-56insACTG	ENSP00000458930.1:n.61-57_61-56insACTG
NM_000160.4:c.61-57_61-56insACTG	NP_000151.1:n.61-57_61-56insACTG
XM_006722277.1:c.61-57_61-56insACTG	XP_006722340.1:n.61-57_61-56insACTG
XM_011523539.1:c.-166-57_-166-56insACTG	XP_011521841.1:n.-166-57_-166-56insACTG
XM_011523540.1:c.-456-57_-456-56insACTG	XP_011521842.1:n.-456-57_-456-56insACTG
XM_017024446.1:c.61-63_61-62insACTG	XP_016879935.1:n.61-63_61-62insACTG
XM_017024447.1:c.-450-63_-450-62insACTG	XP_016879936.1:n.-450-63_-450-62insACTG
NM_000160.5:c.61-57_61-56insACTG MANE Select	NP_000151.1:n.61-57_61-56insACTG