Canonical Allele Identifier: CA1226666982

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704100_230704101delinsAC , CM000663.2:g.230704100_230704101delinsAC	GRCh38
NC_000001.10:g.230839846_230839847delinsAC , CM000663.1:g.230839846_230839847delinsAC	GRCh37
NC_000001.9:g.228906469_228906470delinsAC	NCBI36
NG_008836.1:g.15490_15491delinsGT
NG_008836.2:g.15490_15491delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1242+92_1242+93delinsGT MANE Select	ENSP00000355627.5:n.1242+92_1242+93delinsGT
ENST00000679684.1:c.1242+92_1242+93delinsGT	ENSP00000505981.1:n.1242+92_1242+93delinsGT
ENST00000679738.1:c.1242+92_1242+93delinsGT	ENSP00000505063.1:n.1242+92_1242+93delinsGT
ENST00000679802.1:c.*701+92_*701+93delinsGT	ENSP00000505184.1:n.*701+92_*701+93delinsGT
ENST00000679854.1:n.5547+92_5547+93delinsGT
ENST00000679957.1:c.1233+101_1233+102delinsGT	ENSP00000506646.1:n.1233+101_1233+102delinsGT
ENST00000680041.1:c.1242+92_1242+93delinsGT	ENSP00000504866.1:n.1242+92_1242+93delinsGT
ENST00000680783.1:c.829+5894_829+5895delinsGT	ENSP00000506329.1:n.829+5894_829+5895delinsGT
ENST00000681269.1:c.1242+92_1242+93delinsGT	ENSP00000505985.1:n.1242+92_1242+93delinsGT
ENST00000681347.1:n.3348+92_3348+93delinsGT
ENST00000681514.1:c.1242+92_1242+93delinsGT	ENSP00000505963.1:n.1242+92_1242+93delinsGT
ENST00000681772.1:c.*736+92_*736+93delinsGT	ENSP00000505829.1:n.*736+92_*736+93delinsGT
ENST00000366667.4:c.1269+92_1269+93delinsGT	ENSP00000355627.4:n.1269+92_1269+93delinsGT
NM_000029.3:c.1269+92_1269+93delinsGT	NP_000020.1:n.1269+92_1269+93delinsGT
NM_000029.4:c.1269+92_1269+93delinsGT	NP_000020.1:n.1269+92_1269+93delinsGT
NM_001382817.3:c.1242+92_1242+93delinsGT	NP_001369746.2:n.1242+92_1242+93delinsGT
NM_001384479.1:c.1242+92_1242+93delinsGT MANE Select	NP_001371408.1:n.1242+92_1242+93delinsGT