Canonical Allele Identifier: CA2640508949

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809977-CTTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809978_81809981del , CM000679.2:g.81809978_81809981del	GRCh38
NC_000017.10:g.79767854_79767857del , CM000679.1:g.79767854_79767857del	GRCh37
NG_016409.1:g.8805_8808del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+94_163+97del MANE Select	ENSP00000383558.3:n.163+94_163+97del
ENST00000400723.7:c.163+94_163+97del	ENSP00000383558.3:n.163+94_163+97del
ENST00000570996.5:c.163+94_163+97del	ENSP00000460976.1:n.163+94_163+97del
ENST00000572185.1:n.552_555del
ENST00000573428.1:c.163+94_163+97del	ENSP00000458930.1:n.163+94_163+97del
ENST00000574283.2:n.191_194del
NM_000160.4:c.163+94_163+97del	NP_000151.1:n.163+94_163+97del
XM_006722277.1:c.163+94_163+97del	XP_006722340.1:n.163+94_163+97del
XM_011523539.1:c.31_34del	XP_011521841.1:p.Phe11ArgfsTer?
XM_011523540.1:c.-260_-257del	XP_011521842.1:n.-260_-257del
XM_017024446.1:c.157+94_157+97del	XP_016879935.1:n.157+94_157+97del
XM_017024447.1:c.-260_-257del	XP_016879936.1:n.-260_-257del
NM_000160.5:c.163+94_163+97del MANE Select	NP_000151.1:n.163+94_163+97del