Canonical Allele Identifier: CA1144229232

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703309_230703316delinsAAAAAAAA , CM000663.2:g.230703309_230703316delinsAAAAAAAA	GRCh38
NC_000001.10:g.230839055_230839062delinsAAAAAAAA , CM000663.1:g.230839055_230839062delinsAAAAAAAA	GRCh37
NC_000001.9:g.228905678_228905685delinsAAAAAAAA	NCBI36
NG_008836.1:g.16275_16282delinsTTTTTTTT
NG_008836.2:g.16275_16282delinsTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1256_1263delinsTTTTTTTT MANE Select	ENSP00000355627.5:p.Ile419=
ENST00000679738.1:c.1256_1263delinsTTTTTTTT	ENSP00000505063.1:p.Ile419=
ENST00000679802.1:c.*715_*722delinsTTTTTTTT	ENSP00000505184.1:n.*715_*722delinsTTTTTTTT
ENST00000679854.1:n.5561_5568delinsTTTTTTTT
ENST00000679957.1:c.1247_1254delinsTTTTTTTT	ENSP00000506646.1:p.Ile416=
ENST00000680041.1:c.1256_1263delinsTTTTTTTT	ENSP00000504866.1:p.Ile419=
ENST00000680783.1:c.829+6679_829+6686delinsTTTTTTTT	ENSP00000506329.1:n.829+6679_829+6686delinsTTTTTTTT
ENST00000681269.1:c.1256_1263delinsTTTTTTTT	ENSP00000505985.1:p.Ile419=
ENST00000681347.1:n.3362_3369delinsTTTTTTTT
ENST00000681514.1:c.1256_1263delinsTTTTTTTT	ENSP00000505963.1:p.Ile419=
ENST00000681772.1:c.*750_*757delinsTTTTTTTT	ENSP00000505829.1:n.*750_*757delinsTTTTTTTT
ENST00000366667.4:c.1283_1290delinsTTTTTTTT	ENSP00000355627.4:p.Ile428=
NM_000029.3:c.1283_1290delinsTTTTTTTT	NP_000020.1:p.Ile428=
NM_000029.4:c.1283_1290delinsTTTTTTTT	NP_000020.1:p.Ile428=
NM_001382817.3:c.1256_1263delinsTTTTTTTT	NP_001369746.2:p.Ile419=
NM_001384479.1:c.1256_1263delinsTTTTTTTT MANE Select	NP_001371408.1:p.Ile419=