Canonical Allele Identifier: CA986871685

Gene: GCGR

Linked Data

• gnomAD v3: 17-81809646-C-CCTGT
• gnomAD v4: 17-81809646-C-CCTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809650_81809653dup , CM000679.2:g.81809650_81809653dup	GRCh38
NC_000017.10:g.79767526_79767529dup , CM000679.1:g.79767526_79767529dup	GRCh37
NG_016409.1:g.8477_8480dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-132_61-129dup MANE Select	ENSP00000383558.3:n.61-132_61-129dup
ENST00000400723.7:c.61-132_61-129dup	ENSP00000383558.3:n.61-132_61-129dup
ENST00000570996.5:c.61-132_61-129dup	ENSP00000460976.1:n.61-132_61-129dup
ENST00000572185.1:n.356-132_356-129dup
ENST00000573428.1:c.61-132_61-129dup	ENSP00000458930.1:n.61-132_61-129dup
NM_000160.4:c.61-132_61-129dup	NP_000151.1:n.61-132_61-129dup
XM_006722277.1:c.61-132_61-129dup	XP_006722340.1:n.61-132_61-129dup
XM_011523539.1:c.-166-132_-166-129dup	XP_011521841.1:n.-166-132_-166-129dup
XM_011523540.1:c.-456-132_-456-129dup	XP_011521842.1:n.-456-132_-456-129dup
XM_017024446.1:c.61-138_61-135dup	XP_016879935.1:n.61-138_61-135dup
XM_017024447.1:c.-450-138_-450-135dup	XP_016879936.1:n.-450-138_-450-135dup
NM_000160.5:c.61-132_61-129dup MANE Select	NP_000151.1:n.61-132_61-129dup