Canonical Allele Identifier: CA345202223

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230838975T>G (hg19) ; chr1:g.230703229T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703229T>G , CM000663.2:g.230703229T>G	GRCh38
NC_000001.10:g.230838975T>G , CM000663.1:g.230838975T>G	GRCh37
NC_000001.9:g.228905598T>G	NCBI36
NG_008836.1:g.16362A>C
NG_008836.2:g.16362A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1343A>C MANE Select	ENSP00000355627.5:p.Asn448Thr
ENST00000679738.1:c.1343A>C	ENSP00000505063.1:p.Asn448Thr
ENST00000679802.1:c.*802A>C	ENSP00000505184.1:n.*802A>C
ENST00000679854.1:n.5648A>C
ENST00000679957.1:c.1334A>C	ENSP00000506646.1:p.Asn445Thr
ENST00000680041.1:c.1343A>C	ENSP00000504866.1:p.Asn448Thr
ENST00000680783.1:c.829+6766A>C	ENSP00000506329.1:n.829+6766A>C
ENST00000681269.1:c.1343A>C	ENSP00000505985.1:p.Asn448Thr
ENST00000681347.1:n.3449A>C
ENST00000681514.1:c.1343A>C	ENSP00000505963.1:p.Asn448Thr
ENST00000681772.1:c.*837A>C	ENSP00000505829.1:n.*837A>C
ENST00000366667.4:c.1370A>C	ENSP00000355627.4:p.Asn457Thr
NM_000029.3:c.1370A>C	NP_000020.1:p.Asn457Thr
NM_000029.4:c.1370A>C	NP_000020.1:p.Asn457Thr
NM_001382817.3:c.1343A>C	NP_001369746.2:p.Asn448Thr
NM_001384479.1:c.1343A>C MANE Select	NP_001371408.1:p.Asn448Thr