Canonical Allele Identifier: CA1448061

Gene: AGT

Linked Data

• dbSNP Id: rs772226813
• ExAC: 1:230839090 ACAT / A
• gnomAD v2: 1-230839090-ACAT-A
• gnomAD v3: 1-230703344-ACAT-A
• gnomAD v4: 1-230703344-ACAT-A
• MyVariant Identifiers: chr1:g.230839091_230839093del (hg19) ; chr1:g.230703345_230703347del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703347_230703349del , CM000663.2:g.230703347_230703349del	GRCh38
NC_000001.10:g.230839093_230839095del , CM000663.1:g.230839093_230839095del	GRCh37
NC_000001.9:g.228905716_228905718del	NCBI36
NG_008836.1:g.16244_16246del
NG_008836.2:g.16244_16246del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1243-18_1243-16del MANE Select	ENSP00000355627.5:n.1243-18_1243-16del
ENST00000679738.1:c.1243-18_1243-16del	ENSP00000505063.1:n.1243-18_1243-16del
ENST00000679802.1:c.*702-18_*702-16del	ENSP00000505184.1:n.*702-18_*702-16del
ENST00000679854.1:n.5548-18_5548-16del
ENST00000679957.1:c.1234-18_1234-16del	ENSP00000506646.1:n.1234-18_1234-16del
ENST00000680041.1:c.1243-18_1243-16del	ENSP00000504866.1:n.1243-18_1243-16del
ENST00000680783.1:c.829+6648_829+6650del	ENSP00000506329.1:n.829+6648_829+6650del
ENST00000681269.1:c.1243-18_1243-16del	ENSP00000505985.1:n.1243-18_1243-16del
ENST00000681347.1:n.3349-18_3349-16del
ENST00000681514.1:c.1243-18_1243-16del	ENSP00000505963.1:n.1243-18_1243-16del
ENST00000681772.1:c.*737-18_*737-16del	ENSP00000505829.1:n.*737-18_*737-16del
ENST00000366667.4:c.1270-18_1270-16del	ENSP00000355627.4:n.1270-18_1270-16del
NM_000029.3:c.1270-18_1270-16del	NP_000020.1:n.1270-18_1270-16del
NM_000029.4:c.1270-18_1270-16del	NP_000020.1:n.1270-18_1270-16del
NM_001382817.3:c.1243-18_1243-16del	NP_001369746.2:n.1243-18_1243-16del
NM_001384479.1:c.1243-18_1243-16del MANE Select	NP_001371408.1:n.1243-18_1243-16del