Canonical Allele Identifier: CA2748085530

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702542del , CM000663.2:g.230702542del	GRCh38
NC_000001.10:g.230838288del , CM000663.1:g.230838288del	GRCh37
NC_000001.9:g.228904911del	NCBI36
NG_008836.1:g.17050del
NG_008836.2:g.17050del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*600del MANE Select	ENSP00000355627.5:n.*600del
ENST00000679738.1:c.*600del	ENSP00000505063.1:n.*600del
ENST00000679802.1:c.*1490del	ENSP00000505184.1:n.*1490del
ENST00000679854.1:n.6336del
ENST00000680041.1:c.*600del	ENSP00000504866.1:n.*600del
ENST00000680783.1:c.829+7454del	ENSP00000506329.1:n.829+7454del
ENST00000681269.1:c.*600del	ENSP00000505985.1:n.*600del
ENST00000681347.1:n.4137del
ENST00000681514.1:c.*600del	ENSP00000505963.1:n.*600del
ENST00000681772.1:c.*1525del	ENSP00000505829.1:n.*1525del
ENST00000366667.4:c.*600del	ENSP00000355627.4:n.*600del
NM_000029.3:c.*600del	NP_000020.1:n.*600del
NM_000029.4:c.*600del	NP_000020.1:n.*600del
NM_001382817.3:c.*600del	NP_001369746.2:n.*600del
NM_001384479.1:c.*600del MANE Select	NP_001371408.1:n.*600del