Canonical Allele Identifier: CA2522000333

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713443_230713444del , CM000663.2:g.230713443_230713444del	GRCh38
NC_000001.10:g.230849189_230849190del , CM000663.1:g.230849189_230849190del	GRCh37
NC_000001.9:g.228915812_228915813del	NCBI36
NG_008836.1:g.6147_6148del
NG_008836.2:g.6147_6148del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+642_-31+643del MANE Select	ENSP00000355627.5:n.-31+642_-31+643del
ENST00000679684.1:c.-31+642_-31+643del	ENSP00000505981.1:n.-31+642_-31+643del
ENST00000679738.1:c.-31+642_-31+643del	ENSP00000505063.1:n.-31+642_-31+643del
ENST00000679802.1:c.-31+642_-31+643del	ENSP00000505184.1:n.-31+642_-31+643del
ENST00000679854.1:n.481+642_481+643del
ENST00000679957.1:c.-31+642_-31+643del	ENSP00000506646.1:n.-31+642_-31+643del
ENST00000680041.1:c.-156+642_-156+643del	ENSP00000504866.1:n.-156+642_-156+643del
ENST00000680783.1:c.-31+642_-31+643del	ENSP00000506329.1:n.-31+642_-31+643del
ENST00000681269.1:c.-30-2591_-30-2590del	ENSP00000505985.1:n.-30-2591_-30-2590del
ENST00000681347.1:n.481+642_481+643del
ENST00000681514.1:c.-117-75_-117-74del	ENSP00000505963.1:n.-117-75_-117-74del
ENST00000681772.1:c.-31+642_-31+643del	ENSP00000505829.1:n.-31+642_-31+643del
ENST00000366667.4:c.-4+642_-4+643del	ENSP00000355627.4:n.-4+642_-4+643del
NM_000029.3:c.-4+642_-4+643del	NP_000020.1:n.-4+642_-4+643del
NM_000029.4:c.-4+642_-4+643del	NP_000020.1:n.-4+642_-4+643del
NM_001382817.3:c.-30-2591_-30-2590del	NP_001369746.2:n.-30-2591_-30-2590del
NM_001384479.1:c.-31+642_-31+643del MANE Select	NP_001371408.1:n.-31+642_-31+643del