Canonical Allele Identifier: CA3044762089

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705930_230705933del , CM000663.2:g.230705930_230705933del	GRCh38
NC_000001.10:g.230841676_230841679del , CM000663.1:g.230841676_230841679del	GRCh37
NC_000001.9:g.228908299_228908302del	NCBI36
NG_008836.1:g.13660_13663del
NG_008836.2:g.13660_13663del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1097+2_1097+5del
ENST00000679684.1:c.1097+2_1097+5del
ENST00000679738.1:c.1097+2_1097+5del
ENST00000679802.1:c.*556+2_*556+5del
ENST00000679854.1:n.5402+2_5402+5del
ENST00000679957.1:c.1097+2_1097+5del
ENST00000680041.1:c.1097+2_1097+5del
ENST00000680783.1:c.829+4064_829+4067del	ENSP00000506329.1:n.829+4064_829+4067del
ENST00000681269.1:c.1097+2_1097+5del
ENST00000681347.1:n.1610_1613del
ENST00000681514.1:c.1097+2_1097+5del
ENST00000681772.1:c.1099_*1del	ENSP00000505829.1:n.[c.1099_*1del;Ter367SerextTer27]
ENST00000366667.4:c.1124+2_1124+5del
NM_000029.3:c.1124+2_1124+5del
NM_000029.4:c.1124+2_1124+5del
NM_001382817.3:c.1097+2_1097+5del
NM_001384479.1:c.1097+2_1097+5del