Canonical Allele Identifier: CA1226669473

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230709800_230709801delinsAG , CM000663.2:g.230709800_230709801delinsAG	GRCh38
NC_000001.10:g.230845546_230845547delinsAG , CM000663.1:g.230845546_230845547delinsAG	GRCh37
NC_000001.9:g.228912169_228912170delinsAG	NCBI36
NG_008836.1:g.9790_9791delinsCT
NG_008836.2:g.9790_9791delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+194_829+195delinsCT MANE Select	ENSP00000355627.5:n.829+194_829+195delins...
ENST00000679684.1:c.829+194_829+195delinsCT	ENSP00000505981.1:n.829+194_829+195delins...
ENST00000679738.1:c.829+194_829+195delinsCT	ENSP00000505063.1:n.829+194_829+195delins...
ENST00000679802.1:c.829+194_829+195delinsCT	ENSP00000505184.1:n.829+194_829+195delins...
ENST00000679854.1:n.1534_1535delinsCT
ENST00000679957.1:c.829+194_829+195delinsCT	ENSP00000506646.1:n.829+194_829+195delins...
ENST00000680041.1:c.829+194_829+195delinsCT	ENSP00000504866.1:n.829+194_829+195delins...
ENST00000680783.1:c.829+194_829+195delinsCT	ENSP00000506329.1:n.829+194_829+195delins...
ENST00000681269.1:c.829+194_829+195delinsCT	ENSP00000505985.1:n.829+194_829+195delins...
ENST00000681347.1:n.1340+194_1340+195delinsCT
ENST00000681514.1:c.829+194_829+195delinsCT	ENSP00000505963.1:n.829+194_829+195delins...
ENST00000681772.1:c.829+194_829+195delinsCT	ENSP00000505829.1:n.829+194_829+195delins...
ENST00000366667.4:c.856+194_856+195delinsCT	ENSP00000355627.4:n.856+194_856+195delins...
NM_000029.3:c.856+194_856+195delinsCT	NP_000020.1:n.856+194_856+195delinsCT
NM_000029.4:c.856+194_856+195delinsCT	NP_000020.1:n.856+194_856+195delinsCT
NM_001382817.3:c.829+194_829+195delinsCT	NP_001369746.2:n.829+194_829+195delinsCT
NM_001384479.1:c.829+194_829+195delinsCT MANE Select	NP_001371408.1:n.829+194_829+195delinsCT