Canonical Allele Identifier: CA2569609496

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809645-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809645_81809646insT , CM000679.2:g.81809645_81809646insT	GRCh38
NC_000017.10:g.79767521_79767522insT , CM000679.1:g.79767521_79767522insT	GRCh37
NG_016409.1:g.8472_8473insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-137_61-136insT MANE Select	ENSP00000383558.3:n.61-137_61-136insT
ENST00000400723.7:c.61-137_61-136insT	ENSP00000383558.3:n.61-137_61-136insT
ENST00000570996.5:c.61-137_61-136insT	ENSP00000460976.1:n.61-137_61-136insT
ENST00000572185.1:n.356-137_356-136insT
ENST00000573428.1:c.61-137_61-136insT	ENSP00000458930.1:n.61-137_61-136insT
NM_000160.4:c.61-137_61-136insT	NP_000151.1:n.61-137_61-136insT
XM_006722277.1:c.61-137_61-136insT	XP_006722340.1:n.61-137_61-136insT
XM_011523539.1:c.-166-137_-166-136insT	XP_011521841.1:n.-166-137_-166-136insT
XM_011523540.1:c.-456-137_-456-136insT	XP_011521842.1:n.-456-137_-456-136insT
XM_017024446.1:c.61-143_61-142insT	XP_016879935.1:n.61-143_61-142insT
XM_017024447.1:c.-450-143_-450-142insT	XP_016879936.1:n.-450-143_-450-142insT
NM_000160.5:c.61-137_61-136insT MANE Select	NP_000151.1:n.61-137_61-136insT