Canonical Allele Identifier: CA916424710

Gene: AGT

Linked Data

• dbSNP Id: rs1571973368

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704358_230704359del , CM000663.2:g.230704358_230704359del	GRCh38
NC_000001.10:g.230840104_230840105del , CM000663.1:g.230840104_230840105del	GRCh37
NC_000001.9:g.228906727_228906728del	NCBI36
NG_008836.1:g.15232_15233del
NG_008836.2:g.15232_15233del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1098-22_1098-21del MANE Select	ENSP00000355627.5:n.1098-22_1098-21del
ENST00000679684.1:c.1098-22_1098-21del	ENSP00000505981.1:n.1098-22_1098-21del
ENST00000679738.1:c.1098-22_1098-21del	ENSP00000505063.1:n.1098-22_1098-21del
ENST00000679802.1:c.*557-22_*557-21del	ENSP00000505184.1:n.*557-22_*557-21del
ENST00000679854.1:n.5403-22_5403-21del
ENST00000679957.1:c.1098-22_1098-21del	ENSP00000506646.1:n.1098-22_1098-21del
ENST00000680041.1:c.1098-22_1098-21del	ENSP00000504866.1:n.1098-22_1098-21del
ENST00000680783.1:c.829+5636_829+5637del	ENSP00000506329.1:n.829+5636_829+5637del
ENST00000681269.1:c.1098-22_1098-21del	ENSP00000505985.1:n.1098-22_1098-21del
ENST00000681347.1:n.3182_3183del
ENST00000681514.1:c.1098-22_1098-21del	ENSP00000505963.1:n.1098-22_1098-21del
ENST00000681772.1:c.*592-22_*592-21del	ENSP00000505829.1:n.*592-22_*592-21del
ENST00000366667.4:c.1125-22_1125-21del	ENSP00000355627.4:n.1125-22_1125-21del
NM_000029.3:c.1125-22_1125-21del	NP_000020.1:n.1125-22_1125-21del
NM_000029.4:c.1125-22_1125-21del	NP_000020.1:n.1125-22_1125-21del
NM_001382817.3:c.1098-22_1098-21del	NP_001369746.2:n.1098-22_1098-21del
NM_001384479.1:c.1098-22_1098-21del MANE Select	NP_001371408.1:n.1098-22_1098-21del