Canonical Allele Identifier: CA1226669730

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710411_230710415delinsTAGAG , CM000663.2:g.230710411_230710415delinsTAGAG	GRCh38
NC_000001.10:g.230846157_230846161delinsTAGAG , CM000663.1:g.230846157_230846161delinsTAGAG	GRCh37
NC_000001.9:g.228912780_228912784delinsTAGAG	NCBI36
NG_008836.1:g.9176_9180delinsCTCTA
NG_008836.2:g.9176_9180delinsCTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.409_413delinsCTCTA MANE Select	ENSP00000355627.5:p.Leu137=
ENST00000679684.1:c.409_413delinsCTCTA	ENSP00000505981.1:p.Leu137=
ENST00000679738.1:c.409_413delinsCTCTA	ENSP00000505063.1:p.Leu137=
ENST00000679802.1:c.409_413delinsCTCTA	ENSP00000505184.1:p.Leu137=
ENST00000679854.1:n.920_924delinsCTCTA
ENST00000679957.1:c.409_413delinsCTCTA	ENSP00000506646.1:p.Leu137=
ENST00000680041.1:c.409_413delinsCTCTA	ENSP00000504866.1:p.Leu137=
ENST00000680783.1:c.409_413delinsCTCTA	ENSP00000506329.1:p.Leu137=
ENST00000681269.1:c.409_413delinsCTCTA	ENSP00000505985.1:p.Leu137=
ENST00000681347.1:n.920_924delinsCTCTA
ENST00000681514.1:c.409_413delinsCTCTA	ENSP00000505963.1:p.Leu137=
ENST00000681772.1:c.409_413delinsCTCTA	ENSP00000505829.1:p.Leu137=
ENST00000366667.4:c.436_440delinsCTCTA	ENSP00000355627.4:p.Leu146=
NM_000029.3:c.436_440delinsCTCTA	NP_000020.1:p.Leu146=
NM_000029.4:c.436_440delinsCTCTA	NP_000020.1:p.Leu146=
NM_001382817.3:c.409_413delinsCTCTA	NP_001369746.2:p.Leu137=
NM_001384479.1:c.409_413delinsCTCTA MANE Select	NP_001371408.1:p.Leu137=