Canonical Allele Identifier: CA2640508811

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809710-C-CCTGTCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809714_81809721dup , CM000679.2:g.81809714_81809721dup	GRCh38
NC_000017.10:g.79767590_79767597dup , CM000679.1:g.79767590_79767597dup	GRCh37
NG_016409.1:g.8541_8548dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-68_61-61dup MANE Select	ENSP00000383558.3:n.61-68_61-61dup
ENST00000400723.7:c.61-68_61-61dup	ENSP00000383558.3:n.61-68_61-61dup
ENST00000570996.5:c.61-68_61-61dup	ENSP00000460976.1:n.61-68_61-61dup
ENST00000572185.1:n.356-68_356-61dup
ENST00000573428.1:c.61-68_61-61dup	ENSP00000458930.1:n.61-68_61-61dup
NM_000160.4:c.61-68_61-61dup	NP_000151.1:n.61-68_61-61dup
XM_006722277.1:c.61-68_61-61dup	XP_006722340.1:n.61-68_61-61dup
XM_011523539.1:c.-166-68_-166-61dup	XP_011521841.1:n.-166-68_-166-61dup
XM_011523540.1:c.-456-68_-456-61dup	XP_011521842.1:n.-456-68_-456-61dup
XM_017024446.1:c.61-74_61-67dup	XP_016879935.1:n.61-74_61-67dup
XM_017024447.1:c.-450-74_-450-67dup	XP_016879936.1:n.-450-74_-450-67dup
NM_000160.5:c.61-68_61-61dup MANE Select	NP_000151.1:n.61-68_61-61dup