Canonical Allele Identifier: CA2574012365

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703315_230703316del , CM000663.2:g.230703315_230703316del	GRCh38
NC_000001.10:g.230839061_230839062del , CM000663.1:g.230839061_230839062del	GRCh37
NC_000001.9:g.228905684_228905685del	NCBI36
NG_008836.1:g.16281_16282del
NG_008836.2:g.16281_16282del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1262_1263del MANE Select	ENSP00000355627.5:p.Phe421Ter
ENST00000679738.1:c.1262_1263del	ENSP00000505063.1:p.Phe421Ter
ENST00000679802.1:c.*721_*722del	ENSP00000505184.1:n.*721_*722del
ENST00000679854.1:n.5567_5568del
ENST00000679957.1:c.1253_1254del	ENSP00000506646.1:p.Phe418Ter
ENST00000680041.1:c.1262_1263del	ENSP00000504866.1:p.Phe421Ter
ENST00000680783.1:c.829+6685_829+6686del	ENSP00000506329.1:n.829+6685_829+6686del
ENST00000681269.1:c.1262_1263del	ENSP00000505985.1:p.Phe421Ter
ENST00000681347.1:n.3368_3369del
ENST00000681514.1:c.1262_1263del	ENSP00000505963.1:p.Phe421Ter
ENST00000681772.1:c.*756_*757del	ENSP00000505829.1:n.*756_*757del
ENST00000366667.4:c.1289_1290del	ENSP00000355627.4:p.Phe430Ter
NM_000029.3:c.1289_1290del	NP_000020.1:p.Phe430Ter
NM_000029.4:c.1289_1290del	NP_000020.1:p.Phe430Ter
NM_001382817.3:c.1262_1263del	NP_001369746.2:p.Phe421Ter
NM_001384479.1:c.1262_1263del MANE Select	NP_001371408.1:p.Phe421Ter