Canonical Allele Identifier: CA1226668880

Gene: AGT

Linked Data

• dbSNP Id: rs1663456214

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230708436_230708451dup , CM000663.2:g.230708436_230708451dup	GRCh38
NC_000001.10:g.230844182_230844197dup , CM000663.1:g.230844182_230844197dup	GRCh37
NC_000001.9:g.228910805_228910820dup	NCBI36
NG_008836.1:g.11141_11156dup
NG_008836.2:g.11141_11156dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+1545_829+1560dup MANE Select	ENSP00000355627.5:n.829+1545_829+1560dup
ENST00000679684.1:c.829+1545_829+1560dup	ENSP00000505981.1:n.829+1545_829+1560dup
ENST00000679738.1:c.829+1545_829+1560dup	ENSP00000505063.1:n.829+1545_829+1560dup
ENST00000679802.1:c.*288+657_*288+672dup	ENSP00000505184.1:n.*288+657_*288+672dup
ENST00000679854.1:n.2885_2900dup
ENST00000679957.1:c.829+1545_829+1560dup	ENSP00000506646.1:n.829+1545_829+1560dup
ENST00000680041.1:c.829+1545_829+1560dup	ENSP00000504866.1:n.829+1545_829+1560dup
ENST00000680783.1:c.829+1545_829+1560dup	ENSP00000506329.1:n.829+1545_829+1560dup
ENST00000681269.1:c.829+1545_829+1560dup	ENSP00000505985.1:n.829+1545_829+1560dup
ENST00000681347.1:n.1340+1545_1340+1560dup
ENST00000681514.1:c.829+1545_829+1560dup	ENSP00000505963.1:n.829+1545_829+1560dup
ENST00000681772.1:c.829+1545_829+1560dup	ENSP00000505829.1:n.829+1545_829+1560dup
ENST00000366667.4:c.856+1545_856+1560dup	ENSP00000355627.4:n.856+1545_856+1560dup
NM_000029.3:c.856+1545_856+1560dup	NP_000020.1:n.856+1545_856+1560dup
NM_000029.4:c.856+1545_856+1560dup	NP_000020.1:n.856+1545_856+1560dup
NM_001382817.3:c.829+1545_829+1560dup	NP_001369746.2:n.829+1545_829+1560dup
NM_001384479.1:c.829+1545_829+1560dup MANE Select	NP_001371408.1:n.829+1545_829+1560dup