Canonical Allele Identifier: CA2698274113

Gene: AGT

Linked Data

• dbSNP Id: rs2102791563

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710835del , CM000663.2:g.230710835del	GRCh38
NC_000001.10:g.230846581del , CM000663.1:g.230846581del	GRCh37
NC_000001.9:g.228913204del	NCBI36
NG_008836.1:g.8759del
NG_008836.2:g.8759del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-9del MANE Select	ENSP00000355627.5:n.-9del
ENST00000679684.1:c.-9del	ENSP00000505981.1:n.-9del
ENST00000679738.1:c.-9del	ENSP00000505063.1:n.-9del
ENST00000679802.1:c.-9del	ENSP00000505184.1:n.-9del
ENST00000679854.1:n.503del
ENST00000679957.1:c.-9del	ENSP00000506646.1:n.-9del
ENST00000680041.1:c.-9del	ENSP00000504866.1:n.-9del
ENST00000680783.1:c.-9del	ENSP00000506329.1:n.-9del
ENST00000681269.1:c.-9del	ENSP00000505985.1:n.-9del
ENST00000681347.1:n.503del
ENST00000681514.1:c.-9del	ENSP00000505963.1:n.-9del
ENST00000681772.1:c.-9del	ENSP00000505829.1:n.-9del
ENST00000366667.4:c.19del	ENSP00000355627.4:p.Gln7SerfsTer9
NM_000029.3:c.19del	NP_000020.1:p.Gln7SerfsTer9
NM_000029.4:c.19del	NP_000020.1:p.Gln7SerfsTer9
NM_001382817.3:c.-9del	NP_001369746.2:n.-9del
NM_001384479.1:c.-9del MANE Select	NP_001371408.1:n.-9del