Canonical Allele Identifier: CA2573051513

Gene: AGT

Linked Data

• ClinVar Variation Id: 1328401
• ClinVar RCV Id: RCV001807655
• dbSNP Id: rs2102791328

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710662_230710663delinsA , CM000663.2:g.230710662_230710663delinsA	GRCh38
NC_000001.10:g.230846408_230846409delinsA , CM000663.1:g.230846408_230846409delinsA	GRCh37
NC_000001.9:g.228913031_228913032delinsA	NCBI36
NG_008836.1:g.8928_8929delinsT
NG_008836.2:g.8928_8929delinsT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.161_162delinsT MANE Select	ENSP00000355627.5:p.Lys54MetfsTer28
ENST00000679684.1:c.161_162delinsT	ENSP00000505981.1:p.Lys54MetfsTer28
ENST00000679738.1:c.161_162delinsT	ENSP00000505063.1:p.Lys54MetfsTer28
ENST00000679802.1:c.161_162delinsT	ENSP00000505184.1:p.Lys54MetfsTer28
ENST00000679854.1:n.672_673delinsT
ENST00000679957.1:c.161_162delinsT	ENSP00000506646.1:p.Lys54MetfsTer28
ENST00000680041.1:c.161_162delinsT	ENSP00000504866.1:p.Lys54MetfsTer28
ENST00000680783.1:c.161_162delinsT	ENSP00000506329.1:p.Lys54MetfsTer28
ENST00000681269.1:c.161_162delinsT	ENSP00000505985.1:p.Lys54MetfsTer28
ENST00000681347.1:n.672_673delinsT
ENST00000681514.1:c.161_162delinsT	ENSP00000505963.1:p.Lys54MetfsTer28
ENST00000681772.1:c.161_162delinsT	ENSP00000505829.1:p.Lys54MetfsTer28
ENST00000366667.4:c.188_189delinsT	ENSP00000355627.4:p.Lys63MetfsTer28
NM_000029.3:c.188_189delinsT	NP_000020.1:p.Lys63MetfsTer28
NM_000029.4:c.188_189delinsT	NP_000020.1:p.Lys63MetfsTer28
NM_001382817.3:c.161_162delinsT	NP_001369746.2:p.Lys54MetfsTer28
NM_001384479.1:c.161_162delinsT MANE Select	NP_001371408.1:p.Lys54MetfsTer28