Canonical Allele Identifier: CA919909612

Gene: GCGR

Linked Data

• dbSNP Id: rs370693011
• gnomAD v4: 17-81809889-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809895dup , CM000679.2:g.81809895dup	GRCh38
NC_000017.10:g.79767771dup , CM000679.1:g.79767771dup	GRCh37
NG_016409.1:g.8722dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+11dup MANE Select	ENSP00000383558.3:n.163+11dup
ENST00000400723.7:c.163+11dup	ENSP00000383558.3:n.163+11dup
ENST00000570996.5:c.163+11dup	ENSP00000460976.1:n.163+11dup
ENST00000572185.1:n.469dup
ENST00000573428.1:c.163+11dup	ENSP00000458930.1:n.163+11dup
ENST00000574283.2:n.108dup
NM_000160.4:c.163+11dup	NP_000151.1:n.163+11dup
XM_006722277.1:c.163+11dup	XP_006722340.1:n.163+11dup
XM_011523539.1:c.-53dup	XP_011521841.1:n.-53dup
XM_011523540.1:c.-343dup	XP_011521842.1:n.-343dup
XM_017024446.1:c.157+11dup	XP_016879935.1:n.157+11dup
XM_017024447.1:c.-343dup	XP_016879936.1:n.-343dup
NM_000160.5:c.163+11dup MANE Select	NP_000151.1:n.163+11dup