Canonical Allele Identifier: CA1226667692

Gene: AGT

Linked Data

• dbSNP Id: rs1407711084

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705779_230705782dup , CM000663.2:g.230705779_230705782dup	GRCh38
NC_000001.10:g.230841525_230841528dup , CM000663.1:g.230841525_230841528dup	GRCh37
NC_000001.9:g.228908148_228908151dup	NCBI36
NG_008836.1:g.13814_13817dup
NG_008836.2:g.13814_13817dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+156_1097+159dup MANE Select	ENSP00000355627.5:n.1097+156_1097+159dup
ENST00000679684.1:c.1097+156_1097+159dup	ENSP00000505981.1:n.1097+156_1097+159dup
ENST00000679738.1:c.1097+156_1097+159dup	ENSP00000505063.1:n.1097+156_1097+159dup
ENST00000679802.1:c.*556+156_*556+159dup	ENSP00000505184.1:n.*556+156_*556+159dup
ENST00000679854.1:n.5402+156_5402+159dup
ENST00000679957.1:c.1097+156_1097+159dup	ENSP00000506646.1:n.1097+156_1097+159dup
ENST00000680041.1:c.1097+156_1097+159dup	ENSP00000504866.1:n.1097+156_1097+159dup
ENST00000680783.1:c.829+4218_829+4221dup	ENSP00000506329.1:n.829+4218_829+4221dup
ENST00000681269.1:c.1097+156_1097+159dup	ENSP00000505985.1:n.1097+156_1097+159dup
ENST00000681347.1:n.1764_1767dup
ENST00000681514.1:c.1097+156_1097+159dup	ENSP00000505963.1:n.1097+156_1097+159dup
ENST00000681772.1:c.*152_*155dup	ENSP00000505829.1:n.*152_*155dup
ENST00000366667.4:c.1124+156_1124+159dup	ENSP00000355627.4:n.1124+156_1124+159dup
NM_000029.3:c.1124+156_1124+159dup	NP_000020.1:n.1124+156_1124+159dup
NM_000029.4:c.1124+156_1124+159dup	NP_000020.1:n.1124+156_1124+159dup
NM_001382817.3:c.1097+156_1097+159dup	NP_001369746.2:n.1097+156_1097+159dup
NM_001384479.1:c.1097+156_1097+159dup MANE Select	NP_001371408.1:n.1097+156_1097+159dup