Canonical Allele Identifier: CA1226666957

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704052C= , CM000663.2:g.230704052C=	GRCh38
NC_000001.10:g.230839798C= , CM000663.1:g.230839798C=	GRCh37
NC_000001.9:g.228906421C=	NCBI36
NG_008836.1:g.15539G=
NG_008836.2:g.15539G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1242+141G= MANE Select	ENSP00000355627.5:n.1242+141G=
ENST00000679684.1:c.1243-124G=	ENSP00000505981.1:n.1243-124G=
ENST00000679738.1:c.1242+141G=	ENSP00000505063.1:n.1242+141G=
ENST00000679802.1:c.*701+141G=	ENSP00000505184.1:n.*701+141G=
ENST00000679854.1:n.5547+141G=
ENST00000679957.1:c.1233+150G=	ENSP00000506646.1:n.1233+150G=
ENST00000680041.1:c.1242+141G=	ENSP00000504866.1:n.1242+141G=
ENST00000680783.1:c.829+5943G=	ENSP00000506329.1:n.829+5943G=
ENST00000681269.1:c.1242+141G=	ENSP00000505985.1:n.1242+141G=
ENST00000681347.1:n.3348+141G=
ENST00000681514.1:c.1242+141G=	ENSP00000505963.1:n.1242+141G=
ENST00000681772.1:c.*736+141G=	ENSP00000505829.1:n.*736+141G=
ENST00000366667.4:c.1269+141G=	ENSP00000355627.4:n.1269+141G=
NM_000029.3:c.1269+141G=	NP_000020.1:n.1269+141G=
NM_000029.4:c.1269+141G=	NP_000020.1:n.1269+141G=
NM_001382817.3:c.1242+141G=	NP_001369746.2:n.1242+141G=
NM_001384479.1:c.1242+141G= MANE Select	NP_001371408.1:n.1242+141G=