Canonical Allele Identifier: CA1448126

Gene: AGT

Linked Data

• dbSNP Id: rs769707053
• ExAC: 1:230840119 CCACA / C
• gnomAD v2: 1-230840119-CCACA-C
• gnomAD v4: 1-230704373-CCACA-C
• MyVariant Identifiers: chr1:g.230840120_230840123del (hg19) ; chr1:g.230704374_230704377del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704376_230704379del , CM000663.2:g.230704376_230704379del	GRCh38
NC_000001.10:g.230840122_230840125del , CM000663.1:g.230840122_230840125del	GRCh37
NC_000001.9:g.228906745_228906748del	NCBI36
NG_008836.1:g.15214_15217del
NG_008836.2:g.15214_15217del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1098-40_1098-37del MANE Select	ENSP00000355627.5:n.1098-40_1098-37del
ENST00000679684.1:c.1098-40_1098-37del	ENSP00000505981.1:n.1098-40_1098-37del
ENST00000679738.1:c.1098-40_1098-37del	ENSP00000505063.1:n.1098-40_1098-37del
ENST00000679802.1:c.*557-40_*557-37del	ENSP00000505184.1:n.*557-40_*557-37del
ENST00000679854.1:n.5403-40_5403-37del
ENST00000679957.1:c.1098-40_1098-37del	ENSP00000506646.1:n.1098-40_1098-37del
ENST00000680041.1:c.1098-40_1098-37del	ENSP00000504866.1:n.1098-40_1098-37del
ENST00000680783.1:c.829+5618_829+5621del	ENSP00000506329.1:n.829+5618_829+5621del
ENST00000681269.1:c.1098-40_1098-37del	ENSP00000505985.1:n.1098-40_1098-37del
ENST00000681347.1:n.3164_3167del
ENST00000681514.1:c.1098-40_1098-37del	ENSP00000505963.1:n.1098-40_1098-37del
ENST00000681772.1:c.*592-40_*592-37del	ENSP00000505829.1:n.*592-40_*592-37del
ENST00000366667.4:c.1125-40_1125-37del	ENSP00000355627.4:n.1125-40_1125-37del
NM_000029.3:c.1125-40_1125-37del	NP_000020.1:n.1125-40_1125-37del
NM_000029.4:c.1125-40_1125-37del	NP_000020.1:n.1125-40_1125-37del
NM_001382817.3:c.1098-40_1098-37del	NP_001369746.2:n.1098-40_1098-37del
NM_001384479.1:c.1098-40_1098-37del MANE Select	NP_001371408.1:n.1098-40_1098-37del