Canonical Allele Identifier: CA1226667733

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705861_230705862delinsTC , CM000663.2:g.230705861_230705862delinsTC	GRCh38
NC_000001.10:g.230841607_230841608delinsTC , CM000663.1:g.230841607_230841608delinsTC	GRCh37
NC_000001.9:g.228908230_228908231delinsTC	NCBI36
NG_008836.1:g.13729_13730delinsGA
NG_008836.2:g.13729_13730delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+71_1097+72delinsGA MANE Select	ENSP00000355627.5:n.1097+71_1097+72delins...
ENST00000679684.1:c.1097+71_1097+72delinsGA	ENSP00000505981.1:n.1097+71_1097+72delins...
ENST00000679738.1:c.1097+71_1097+72delinsGA	ENSP00000505063.1:n.1097+71_1097+72delins...
ENST00000679802.1:c.*556+71_*556+72delinsGA	ENSP00000505184.1:n.*556+71_*556+72delins...
ENST00000679854.1:n.5402+71_5402+72delinsGA
ENST00000679957.1:c.1097+71_1097+72delinsGA	ENSP00000506646.1:n.1097+71_1097+72delins...
ENST00000680041.1:c.1097+71_1097+72delinsGA	ENSP00000504866.1:n.1097+71_1097+72delins...
ENST00000680783.1:c.829+4133_829+4134delinsGA	ENSP00000506329.1:n.829+4133_829+4134deli...
ENST00000681269.1:c.1097+71_1097+72delinsGA	ENSP00000505985.1:n.1097+71_1097+72delins...
ENST00000681347.1:n.1679_1680delinsGA
ENST00000681514.1:c.1097+71_1097+72delinsGA	ENSP00000505963.1:n.1097+71_1097+72delins...
ENST00000681772.1:c.*67_*68delinsGA	ENSP00000505829.1:n.*67_*68delinsGA
ENST00000366667.4:c.1124+71_1124+72delinsGA	ENSP00000355627.4:n.1124+71_1124+72delins...
NM_000029.3:c.1124+71_1124+72delinsGA	NP_000020.1:n.1124+71_1124+72delinsGA
NM_000029.4:c.1124+71_1124+72delinsGA	NP_000020.1:n.1124+71_1124+72delinsGA
NM_001382817.3:c.1097+71_1097+72delinsGA	NP_001369746.2:n.1097+71_1097+72delinsGA
NM_001384479.1:c.1097+71_1097+72delinsGA MANE Select	NP_001371408.1:n.1097+71_1097+72delinsGA