Canonical Allele Identifier: CA2576426173

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809881-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809882del , CM000679.2:g.81809882del	GRCh38
NC_000017.10:g.79767758del , CM000679.1:g.79767758del	GRCh37
NG_016409.1:g.8709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.161del MANE Select	ENSP00000383558.3:p.Thr54ArgfsTer?
ENST00000400723.7:c.161del	ENSP00000383558.3:p.Thr54ArgfsTer?
ENST00000570996.5:c.161del	ENSP00000460976.1:p.Thr54ArgfsTer?
ENST00000572185.1:n.456del
ENST00000573428.1:c.161del	ENSP00000458930.1:p.Thr54ArgfsTer?
ENST00000574283.2:n.95del
NM_000160.4:c.161del	NP_000151.1:p.Thr54ArgfsTer?
XM_006722277.1:c.161del	XP_006722340.1:p.Thr54ArgfsTer?
XM_011523539.1:c.-66del	XP_011521841.1:n.-66del
XM_011523540.1:c.-356del	XP_011521842.1:n.-356del
XM_017024446.1:c.155del	XP_016879935.1:p.Thr52ArgfsTer?
XM_017024447.1:c.-356del	XP_016879936.1:n.-356del
NM_000160.5:c.161del MANE Select	NP_000151.1:p.Thr54ArgfsTer?