Canonical Allele Identifier: CA345202478

Gene: AGT

Linked Data

• gnomAD v4: 1-230703284-G-C
• MyVariant Identifiers: chr1:g.230839030G>C (hg19) ; chr1:g.230703284G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703284G>C , CM000663.2:g.230703284G>C	GRCh38
NC_000001.10:g.230839030G>C , CM000663.1:g.230839030G>C	GRCh37
NC_000001.9:g.228905653G>C	NCBI36
NG_008836.1:g.16307C>G
NG_008836.2:g.16307C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1288C>G MANE Select	ENSP00000355627.5:p.Pro430Ala
ENST00000679738.1:c.1288C>G	ENSP00000505063.1:p.Pro430Ala
ENST00000679802.1:c.*747C>G	ENSP00000505184.1:n.*747C>G
ENST00000679854.1:n.5593C>G
ENST00000679957.1:c.1279C>G	ENSP00000506646.1:p.Pro427Ala
ENST00000680041.1:c.1288C>G	ENSP00000504866.1:p.Pro430Ala
ENST00000680783.1:c.829+6711C>G	ENSP00000506329.1:n.829+6711C>G
ENST00000681269.1:c.1288C>G	ENSP00000505985.1:p.Pro430Ala
ENST00000681347.1:n.3394C>G
ENST00000681514.1:c.1288C>G	ENSP00000505963.1:p.Pro430Ala
ENST00000681772.1:c.*782C>G	ENSP00000505829.1:n.*782C>G
ENST00000366667.4:c.1315C>G	ENSP00000355627.4:p.Pro439Ala
NM_000029.3:c.1315C>G	NP_000020.1:p.Pro439Ala
NM_000029.4:c.1315C>G	NP_000020.1:p.Pro439Ala
NM_001382817.3:c.1288C>G	NP_001369746.2:p.Pro430Ala
NM_001384479.1:c.1288C>G MANE Select	NP_001371408.1:p.Pro430Ala