Canonical Allele Identifier: CA645521367

Gene: AGT

Linked Data

• COSMIC: COSM4603074

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704251_230704252insGGC , CM000663.2:g.230704251_230704252insGGC	GRCh38
NC_000001.10:g.230839997_230839998insGGC , CM000663.1:g.230839997_230839998insGGC	GRCh37
NC_000001.9:g.228906620_228906621insGGC	NCBI36
NG_008836.1:g.15339_15340insGCC
NG_008836.2:g.15339_15340insGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1183_1184insGCC MANE Select	ENSP00000355627.5:p.Ile395delinsSerLeu
ENST00000679684.1:c.1183_1184insGCC	ENSP00000505981.1:p.Ile395delinsSerLeu
ENST00000679738.1:c.1183_1184insGCC	ENSP00000505063.1:p.Ile395delinsSerLeu
ENST00000679802.1:c.*642_*643insGCC	ENSP00000505184.1:n.*642_*643insGCC
ENST00000679854.1:n.5488_5489insGCC
ENST00000679957.1:c.1183_1184insGCC	ENSP00000506646.1:p.Ile395delinsSerLeu
ENST00000680041.1:c.1183_1184insGCC	ENSP00000504866.1:p.Ile395delinsSerLeu
ENST00000680783.1:c.829+5743_829+5744insGCC	ENSP00000506329.1:n.829+5743_829+5744insG...
ENST00000681269.1:c.1183_1184insGCC	ENSP00000505985.1:p.Ile395delinsSerLeu
ENST00000681347.1:n.3289_3290insGCC
ENST00000681514.1:c.1183_1184insGCC	ENSP00000505963.1:p.Ile395delinsSerLeu
ENST00000681772.1:c.*677_*678insGCC	ENSP00000505829.1:n.*677_*678insGCC
ENST00000366667.4:c.1210_1211insGCC	ENSP00000355627.4:p.Ile404delinsSerLeu
NM_000029.3:c.1210_1211insGCC	NP_000020.1:p.Ile404delinsSerLeu
NM_000029.4:c.1210_1211insGCC	NP_000020.1:p.Ile404delinsSerLeu
NM_001382817.3:c.1183_1184insGCC	NP_001369746.2:p.Ile395delinsSerLeu
NM_001384479.1:c.1183_1184insGCC MANE Select	NP_001371408.1:p.Ile395delinsSerLeu