Canonical Allele Identifier: CA2573684383

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704201_230704202insT , CM000663.2:g.230704201_230704202insT	GRCh38
NC_000001.10:g.230839947_230839948insT , CM000663.1:g.230839947_230839948insT	GRCh37
NC_000001.9:g.228906570_228906571insT	NCBI36
NG_008836.1:g.15389_15390insA
NG_008836.2:g.15389_15390insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1233_1234insA MANE Select	ENSP00000355627.5:p.Val412SerfsTer11
ENST00000679684.1:c.1233_1234insA	ENSP00000505981.1:p.Val412SerfsTer17
ENST00000679738.1:c.1233_1234insA	ENSP00000505063.1:p.Val412SerfsTer11
ENST00000679802.1:c.*692_*693insA	ENSP00000505184.1:n.*692_*693insA
ENST00000679854.1:n.5538_5539insA
ENST00000679957.1:c.1233_1233+1insA	ENSP00000506646.1:n.1233_1233+1insA
ENST00000680041.1:c.1233_1234insA	ENSP00000504866.1:p.Val412SerfsTer11
ENST00000680783.1:c.829+5793_829+5794insA	ENSP00000506329.1:n.829+5793_829+5794insA
ENST00000681269.1:c.1233_1234insA	ENSP00000505985.1:p.Val412SerfsTer11
ENST00000681347.1:n.3339_3340insA
ENST00000681514.1:c.1233_1234insA	ENSP00000505963.1:p.Val412SerfsTer11
ENST00000681772.1:c.*727_*728insA	ENSP00000505829.1:n.*727_*728insA
ENST00000366667.4:c.1260_1261insA	ENSP00000355627.4:p.Val421SerfsTer11
NM_000029.3:c.1260_1261insA	NP_000020.1:p.Val421SerfsTer11
NM_000029.4:c.1260_1261insA	NP_000020.1:p.Val421SerfsTer11
NM_001382817.3:c.1233_1234insA	NP_001369746.2:p.Val412SerfsTer11
NM_001384479.1:c.1233_1234insA MANE Select	NP_001371408.1:p.Val412SerfsTer11