Canonical Allele Identifier: CA529691739

Gene: AGT

Linked Data

• dbSNP Id: rs1440283827
• gnomAD v2: 1-230849677-GGGGAAAGCCCGCGTCC-G
• gnomAD v3: 1-230713931-GGGGAAAGCCCGCGTCC-G
• gnomAD v4: 1-230713931-GGGGAAAGCCCGCGTCC-G
• MyVariant Identifiers: chr1:g.230849678_230849693del (hg19) ; chr1:g.230713932_230713947del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713934_230713949del , CM000663.2:g.230713934_230713949del	GRCh38
NC_000001.10:g.230849680_230849695del , CM000663.1:g.230849680_230849695del	GRCh37
NC_000001.9:g.228916303_228916318del	NCBI36
NG_008836.1:g.5644_5659del
NG_008836.2:g.5644_5659del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+139_-31+154del MANE Select	ENSP00000355627.5:n.-31+139_-31+154del
ENST00000679684.1:c.-31+139_-31+154del	ENSP00000505981.1:n.-31+139_-31+154del
ENST00000679738.1:c.-31+139_-31+154del	ENSP00000505063.1:n.-31+139_-31+154del
ENST00000679802.1:c.-31+139_-31+154del	ENSP00000505184.1:n.-31+139_-31+154del
ENST00000679854.1:n.481+139_481+154del
ENST00000679957.1:c.-31+139_-31+154del	ENSP00000506646.1:n.-31+139_-31+154del
ENST00000680041.1:c.-156+139_-156+154del	ENSP00000504866.1:n.-156+139_-156+154del
ENST00000680783.1:c.-31+139_-31+154del	ENSP00000506329.1:n.-31+139_-31+154del
ENST00000681269.1:c.-30-3094_-30-3079del	ENSP00000505985.1:n.-30-3094_-30-3079del
ENST00000681347.1:n.481+139_481+154del
ENST00000681514.1:c.-118+139_-118+154del	ENSP00000505963.1:n.-118+139_-118+154del
ENST00000681772.1:c.-31+139_-31+154del	ENSP00000505829.1:n.-31+139_-31+154del
ENST00000366667.4:c.-4+139_-4+154del	ENSP00000355627.4:n.-4+139_-4+154del
NM_000029.3:c.-4+139_-4+154del	NP_000020.1:n.-4+139_-4+154del
NM_000029.4:c.-4+139_-4+154del	NP_000020.1:n.-4+139_-4+154del
NM_001382817.3:c.-30-3094_-30-3079del	NP_001369746.2:n.-30-3094_-30-3079del
NM_001384479.1:c.-31+139_-31+154del MANE Select	NP_001371408.1:n.-31+139_-31+154del