Canonical Allele Identifier: CA1226669478

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230709814_230709815delinsAG , CM000663.2:g.230709814_230709815delinsAG	GRCh38
NC_000001.10:g.230845560_230845561delinsAG , CM000663.1:g.230845560_230845561delinsAG	GRCh37
NC_000001.9:g.228912183_228912184delinsAG	NCBI36
NG_008836.1:g.9776_9777delinsCT
NG_008836.2:g.9776_9777delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+180_829+181delinsCT MANE Select	ENSP00000355627.5:n.829+180_829+181delins...
ENST00000679684.1:c.829+180_829+181delinsCT	ENSP00000505981.1:n.829+180_829+181delins...
ENST00000679738.1:c.829+180_829+181delinsCT	ENSP00000505063.1:n.829+180_829+181delins...
ENST00000679802.1:c.829+180_829+181delinsCT	ENSP00000505184.1:n.829+180_829+181delins...
ENST00000679854.1:n.1520_1521delinsCT
ENST00000679957.1:c.829+180_829+181delinsCT	ENSP00000506646.1:n.829+180_829+181delins...
ENST00000680041.1:c.829+180_829+181delinsCT	ENSP00000504866.1:n.829+180_829+181delins...
ENST00000680783.1:c.829+180_829+181delinsCT	ENSP00000506329.1:n.829+180_829+181delins...
ENST00000681269.1:c.829+180_829+181delinsCT	ENSP00000505985.1:n.829+180_829+181delins...
ENST00000681347.1:n.1340+180_1340+181delinsCT
ENST00000681514.1:c.829+180_829+181delinsCT	ENSP00000505963.1:n.829+180_829+181delins...
ENST00000681772.1:c.829+180_829+181delinsCT	ENSP00000505829.1:n.829+180_829+181delins...
ENST00000366667.4:c.856+180_856+181delinsCT	ENSP00000355627.4:n.856+180_856+181delins...
NM_000029.3:c.856+180_856+181delinsCT	NP_000020.1:n.856+180_856+181delinsCT
NM_000029.4:c.856+180_856+181delinsCT	NP_000020.1:n.856+180_856+181delinsCT
NM_001382817.3:c.829+180_829+181delinsCT	NP_001369746.2:n.829+180_829+181delinsCT
NM_001384479.1:c.829+180_829+181delinsCT MANE Select	NP_001371408.1:n.829+180_829+181delinsCT