Canonical Allele Identifier: CA1448045

Gene: AGT

Linked Data

• dbSNP Id: rs756687983
• ExAC: 1:230838974 G / GT
• gnomAD v4: 1-230703228-G-GT
• MyVariant Identifiers: chr1:g.230838974_230838975insT (hg19) ; chr1:g.230703228_230703229insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703230dup , CM000663.2:g.230703230dup	GRCh38
NC_000001.10:g.230838976dup , CM000663.1:g.230838976dup	GRCh37
NC_000001.9:g.228905599dup	NCBI36
NG_008836.1:g.16362dup
NG_008836.2:g.16362dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1343dup MANE Select	ENSP00000355627.5:p.Asn448LysfsTer10
ENST00000679738.1:c.1343dup	ENSP00000505063.1:p.Asn448LysfsTer10
ENST00000679802.1:c.*802dup	ENSP00000505184.1:n.*802dup
ENST00000679854.1:n.5648dup
ENST00000679957.1:c.1334dup	ENSP00000506646.1:p.Asn445LysfsTer10
ENST00000680041.1:c.1343dup	ENSP00000504866.1:p.Asn448LysfsTer10
ENST00000680783.1:c.829+6766dup	ENSP00000506329.1:n.829+6766dup
ENST00000681269.1:c.1343dup	ENSP00000505985.1:p.Asn448LysfsTer10
ENST00000681347.1:n.3449dup
ENST00000681514.1:c.1343dup	ENSP00000505963.1:p.Asn448LysfsTer10
ENST00000681772.1:c.*837dup	ENSP00000505829.1:n.*837dup
ENST00000366667.4:c.1370dup	ENSP00000355627.4:p.Asn457LysfsTer10
NM_000029.3:c.1370dup	NP_000020.1:p.Asn457LysfsTer10
NM_000029.4:c.1370dup	NP_000020.1:p.Asn457LysfsTer10
NM_001382817.3:c.1343dup	NP_001369746.2:p.Asn448LysfsTer10
NM_001384479.1:c.1343dup MANE Select	NP_001371408.1:p.Asn448LysfsTer10