Canonical Allele Identifier: CA1226661730

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713719_230713720delinsTC , CM000663.2:g.230713719_230713720delinsTC	GRCh38
NC_000001.10:g.230849465_230849466delinsTC , CM000663.1:g.230849465_230849466delinsTC	GRCh37
NC_000001.9:g.228916088_228916089delinsTC	NCBI36
NG_008836.1:g.5871_5872delinsGA
NG_008836.2:g.5871_5872delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-31+366_-31+367delinsGA MANE Select	ENSP00000355627.5:n.-31+366_-31+367delinsGA
ENST00000679684.1:c.-31+366_-31+367delinsGA	ENSP00000505981.1:n.-31+366_-31+367delinsGA
ENST00000679738.1:c.-31+366_-31+367delinsGA	ENSP00000505063.1:n.-31+366_-31+367delinsGA
ENST00000679802.1:c.-31+366_-31+367delinsGA	ENSP00000505184.1:n.-31+366_-31+367delinsGA
ENST00000679854.1:n.481+366_481+367delinsGA
ENST00000679957.1:c.-31+366_-31+367delinsGA	ENSP00000506646.1:n.-31+366_-31+367delinsGA
ENST00000680041.1:c.-156+366_-156+367delinsGA	ENSP00000504866.1:n.-156+366_-156+367delinsGA
ENST00000680783.1:c.-31+366_-31+367delinsGA	ENSP00000506329.1:n.-31+366_-31+367delinsGA
ENST00000681269.1:c.-30-2867_-30-2866delinsGA	ENSP00000505985.1:n.-30-2867_-30-2866delinsGA
ENST00000681347.1:n.481+366_481+367delinsGA
ENST00000681514.1:c.-117-351_-117-350delinsGA	ENSP00000505963.1:n.-117-351_-117-350delinsGA
ENST00000681772.1:c.-31+366_-31+367delinsGA	ENSP00000505829.1:n.-31+366_-31+367delinsGA
ENST00000366667.4:c.-4+366_-4+367delinsGA	ENSP00000355627.4:n.-4+366_-4+367delinsGA
NM_000029.3:c.-4+366_-4+367delinsGA	NP_000020.1:n.-4+366_-4+367delinsGA
NM_000029.4:c.-4+366_-4+367delinsGA	NP_000020.1:n.-4+366_-4+367delinsGA
NM_001382817.3:c.-30-2867_-30-2866delinsGA	NP_001369746.2:n.-30-2867_-30-2866delinsGA
NM_001384479.1:c.-31+366_-31+367delinsGA MANE Select	NP_001371408.1:n.-31+366_-31+367delinsGA