Canonical Allele Identifier: CA1448213

Gene: AGT

Linked Data

• dbSNP Id: rs766263902
• ExAC: 1:230841990 CAG / C
• gnomAD v2: 1-230841990-CAG-C
• gnomAD v3: 1-230706244-CAG-C
• gnomAD v4: 1-230706244-CAG-C
• MyVariant Identifiers: chr1:g.230841991_230841992del (hg19) ; chr1:g.230706245_230706246del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230706245_230706246del , CM000663.2:g.230706245_230706246del	GRCh38
NC_000001.10:g.230841991_230841992del , CM000663.1:g.230841991_230841992del	GRCh37
NC_000001.9:g.228908614_228908615del	NCBI36
NG_008836.1:g.13345_13346del
NG_008836.2:g.13345_13346del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.830-46_830-45del MANE Select	ENSP00000355627.5:n.830-46_830-45del
ENST00000679684.1:c.830-46_830-45del	ENSP00000505981.1:n.830-46_830-45del
ENST00000679738.1:c.830-46_830-45del	ENSP00000505063.1:n.830-46_830-45del
ENST00000679802.1:c.*289-46_*289-45del	ENSP00000505184.1:n.*289-46_*289-45del
ENST00000679854.1:n.5089_5090del
ENST00000679957.1:c.830-46_830-45del	ENSP00000506646.1:n.830-46_830-45del
ENST00000680041.1:c.830-46_830-45del	ENSP00000504866.1:n.830-46_830-45del
ENST00000680783.1:c.829+3749_829+3750del	ENSP00000506329.1:n.829+3749_829+3750del
ENST00000681269.1:c.830-46_830-45del	ENSP00000505985.1:n.830-46_830-45del
ENST00000681347.1:n.1341-46_1341-45del
ENST00000681514.1:c.830-46_830-45del	ENSP00000505963.1:n.830-46_830-45del
ENST00000681772.1:c.830-46_830-45del	ENSP00000505829.1:n.830-46_830-45del
ENST00000366667.4:c.857-46_857-45del	ENSP00000355627.4:n.857-46_857-45del
NM_000029.3:c.857-46_857-45del	NP_000020.1:n.857-46_857-45del
NM_000029.4:c.857-46_857-45del	NP_000020.1:n.857-46_857-45del
NM_001382817.3:c.830-46_830-45del	NP_001369746.2:n.830-46_830-45del
NM_001384479.1:c.830-46_830-45del MANE Select	NP_001371408.1:n.830-46_830-45del