Canonical Allele Identifier: CA2640508842

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809734-C-CCTGCCTGTCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809738_81809749dup , CM000679.2:g.81809738_81809749dup	GRCh38
NC_000017.10:g.79767614_79767625dup , CM000679.1:g.79767614_79767625dup	GRCh37
NG_016409.1:g.8565_8576dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-44_61-33dup MANE Select	ENSP00000383558.3:n.61-44_61-33dup
ENST00000400723.7:c.61-44_61-33dup	ENSP00000383558.3:n.61-44_61-33dup
ENST00000570996.5:c.61-44_61-33dup	ENSP00000460976.1:n.61-44_61-33dup
ENST00000572185.1:n.356-44_356-33dup
ENST00000573428.1:c.61-44_61-33dup	ENSP00000458930.1:n.61-44_61-33dup
NM_000160.4:c.61-44_61-33dup	NP_000151.1:n.61-44_61-33dup
XM_006722277.1:c.61-44_61-33dup	XP_006722340.1:n.61-44_61-33dup
XM_011523539.1:c.-166-44_-166-33dup	XP_011521841.1:n.-166-44_-166-33dup
XM_011523540.1:c.-456-44_-456-33dup	XP_011521842.1:n.-456-44_-456-33dup
XM_017024446.1:c.61-50_61-39dup	XP_016879935.1:n.61-50_61-39dup
XM_017024447.1:c.-450-50_-450-39dup	XP_016879936.1:n.-450-50_-450-39dup
NM_000160.5:c.61-44_61-33dup MANE Select	NP_000151.1:n.61-44_61-33dup