Canonical Allele Identifier: CA2278680029

Gene: GCGR

Linked Data

• dbSNP Id: rs2038059760

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809914del , CM000679.2:g.81809914del	GRCh38
NC_000017.10:g.79767790del , CM000679.1:g.79767790del	GRCh37
NG_016409.1:g.8741del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+30del MANE Select	ENSP00000383558.3:n.163+30del
ENST00000400723.7:c.163+30del	ENSP00000383558.3:n.163+30del
ENST00000570996.5:c.163+30del	ENSP00000460976.1:n.163+30del
ENST00000572185.1:n.488del
ENST00000573428.1:c.163+30del	ENSP00000458930.1:n.163+30del
ENST00000574283.2:n.127del
NM_000160.4:c.163+30del	NP_000151.1:n.163+30del
XM_006722277.1:c.163+30del	XP_006722340.1:n.163+30del
XM_011523539.1:c.-34del	XP_011521841.1:n.-34del
XM_011523540.1:c.-324del	XP_011521842.1:n.-324del
XM_017024446.1:c.157+30del	XP_016879935.1:n.157+30del
XM_017024447.1:c.-324del	XP_016879936.1:n.-324del
NM_000160.5:c.163+30del MANE Select	NP_000151.1:n.163+30del