Canonical Allele Identifier: CA1226666998

Gene: AGT

Linked Data

• dbSNP Id: rs1663311679

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704130_230704131dup , CM000663.2:g.230704130_230704131dup	GRCh38
NC_000001.10:g.230839876_230839877dup , CM000663.1:g.230839876_230839877dup	GRCh37
NC_000001.9:g.228906499_228906500dup	NCBI36
NG_008836.1:g.15460_15461dup
NG_008836.2:g.15460_15461dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1242+62_1242+63dup MANE Select	ENSP00000355627.5:n.1242+62_1242+63dup
ENST00000679684.1:c.1242+62_1242+63dup	ENSP00000505981.1:n.1242+62_1242+63dup
ENST00000679738.1:c.1242+62_1242+63dup	ENSP00000505063.1:n.1242+62_1242+63dup
ENST00000679802.1:c.*701+62_*701+63dup	ENSP00000505184.1:n.*701+62_*701+63dup
ENST00000679854.1:n.5547+62_5547+63dup
ENST00000679957.1:c.1233+71_1233+72dup	ENSP00000506646.1:n.1233+71_1233+72dup
ENST00000680041.1:c.1242+62_1242+63dup	ENSP00000504866.1:n.1242+62_1242+63dup
ENST00000680783.1:c.829+5864_829+5865dup	ENSP00000506329.1:n.829+5864_829+5865dup
ENST00000681269.1:c.1242+62_1242+63dup	ENSP00000505985.1:n.1242+62_1242+63dup
ENST00000681347.1:n.3348+62_3348+63dup
ENST00000681514.1:c.1242+62_1242+63dup	ENSP00000505963.1:n.1242+62_1242+63dup
ENST00000681772.1:c.*736+62_*736+63dup	ENSP00000505829.1:n.*736+62_*736+63dup
ENST00000366667.4:c.1269+62_1269+63dup	ENSP00000355627.4:n.1269+62_1269+63dup
NM_000029.3:c.1269+62_1269+63dup	NP_000020.1:n.1269+62_1269+63dup
NM_000029.4:c.1269+62_1269+63dup	NP_000020.1:n.1269+62_1269+63dup
NM_001382817.3:c.1242+62_1242+63dup	NP_001369746.2:n.1242+62_1242+63dup
NM_001384479.1:c.1242+62_1242+63dup MANE Select	NP_001371408.1:n.1242+62_1242+63dup