Canonical Allele Identifier: CA732702103

Gene: AGT

Linked Data

• dbSNP Id: rs1414015619
• gnomAD v3: 1-230708344-GGACCCTCCTTCTCAGT-G
• gnomAD v4: 1-230708344-GGACCCTCCTTCTCAGT-G
• MyVariant Identifiers: chr1:g.230844091_230844106del (hg19) ; chr1:g.230708345_230708360del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230708347_230708362del , CM000663.2:g.230708347_230708362del	GRCh38
NC_000001.10:g.230844093_230844108del , CM000663.1:g.230844093_230844108del	GRCh37
NC_000001.9:g.228910716_228910731del	NCBI36
NG_008836.1:g.11231_11246del
NG_008836.2:g.11231_11246del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+1635_829+1650del MANE Select	ENSP00000355627.5:n.829+1635_829+1650del
ENST00000679684.1:c.829+1635_829+1650del	ENSP00000505981.1:n.829+1635_829+1650del
ENST00000679738.1:c.829+1635_829+1650del	ENSP00000505063.1:n.829+1635_829+1650del
ENST00000679802.1:c.*288+747_*288+762del	ENSP00000505184.1:n.*288+747_*288+762del
ENST00000679854.1:n.2975_2990del
ENST00000679957.1:c.829+1635_829+1650del	ENSP00000506646.1:n.829+1635_829+1650del
ENST00000680041.1:c.829+1635_829+1650del	ENSP00000504866.1:n.829+1635_829+1650del
ENST00000680783.1:c.829+1635_829+1650del	ENSP00000506329.1:n.829+1635_829+1650del
ENST00000681269.1:c.829+1635_829+1650del	ENSP00000505985.1:n.829+1635_829+1650del
ENST00000681347.1:n.1340+1635_1340+1650del
ENST00000681514.1:c.829+1635_829+1650del	ENSP00000505963.1:n.829+1635_829+1650del
ENST00000681772.1:c.829+1635_829+1650del	ENSP00000505829.1:n.829+1635_829+1650del
ENST00000366667.4:c.856+1635_856+1650del	ENSP00000355627.4:n.856+1635_856+1650del
NM_000029.3:c.856+1635_856+1650del	NP_000020.1:n.856+1635_856+1650del
NM_000029.4:c.856+1635_856+1650del	NP_000020.1:n.856+1635_856+1650del
NM_001382817.3:c.829+1635_829+1650del	NP_001369746.2:n.829+1635_829+1650del
NM_001384479.1:c.829+1635_829+1650del MANE Select	NP_001371408.1:n.829+1635_829+1650del