Canonical Allele Identifier: CA2650970691

Gene: AGT

Linked Data

• gnomAD v4: 1-230704190-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704191dup , CM000663.2:g.230704191dup	GRCh38
NC_000001.10:g.230839937dup , CM000663.1:g.230839937dup	GRCh37
NC_000001.9:g.228906560dup	NCBI36
NG_008836.1:g.15400dup
NG_008836.2:g.15400dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1242+2dup MANE Select	ENSP00000355627.5:n.1242+2dup
ENST00000679684.1:c.1242+2dup	ENSP00000505981.1:n.1242+2dup
ENST00000679738.1:c.1242+2dup	ENSP00000505063.1:n.1242+2dup
ENST00000679802.1:c.*701+2dup	ENSP00000505184.1:n.*701+2dup
ENST00000679854.1:n.5547+2dup
ENST00000679957.1:c.1233+11dup	ENSP00000506646.1:n.1233+11dup
ENST00000680041.1:c.1242+2dup	ENSP00000504866.1:n.1242+2dup
ENST00000680783.1:c.829+5804dup	ENSP00000506329.1:n.829+5804dup
ENST00000681269.1:c.1242+2dup	ENSP00000505985.1:n.1242+2dup
ENST00000681347.1:n.3348+2dup
ENST00000681514.1:c.1242+2dup	ENSP00000505963.1:n.1242+2dup
ENST00000681772.1:c.*736+2dup	ENSP00000505829.1:n.*736+2dup
ENST00000366667.4:c.1269+2dup	ENSP00000355627.4:n.1269+2dup
NM_000029.3:c.1269+2dup	NP_000020.1:n.1269+2dup
NM_000029.4:c.1269+2dup	NP_000020.1:n.1269+2dup
NM_001382817.3:c.1242+2dup	NP_001369746.2:n.1242+2dup
NM_001384479.1:c.1242+2dup MANE Select	NP_001371408.1:n.1242+2dup