Canonical Allele Identifier: CA2650971413
Gene: AGT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710302_230710303insCCCTGTACAGCCT , CM000663.2:g.230710302_230710303insCCCTGTACAGCCT GRCh38
NC_000001.10:g.230846048_230846049insCCCTGTACAGCCT , CM000663.1:g.230846048_230846049insCCCTGTACAGCCT GRCh37
NC_000001.9:g.228912671_228912672insCCCTGTACAGCCT NCBI36
NG_008836.1:g.9288_9289insAGGCTGTACAGGG
NG_008836.2:g.9288_9289insAGGCTGTACAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.521_522insAGGCTGTACAGGG MANE Select ENSP00000355627.5:p.Leu175GlyfsTer19
ENST00000679684.1:c.521_522insAGGCTGTACAGGG ENSP00000505981.1:p.Leu175GlyfsTer19
ENST00000679738.1:c.521_522insAGGCTGTACAGGG ENSP00000505063.1:p.Leu175GlyfsTer19
ENST00000679802.1:c.521_522insAGGCTGTACAGGG ENSP00000505184.1:p.Leu175GlyfsTer19
ENST00000679854.1:n.1032_1033insAGGCTGTACAGGG
ENST00000679957.1:c.521_522insAGGCTGTACAGGG ENSP00000506646.1:p.Leu175GlyfsTer19
ENST00000680041.1:c.521_522insAGGCTGTACAGGG ENSP00000504866.1:p.Leu175GlyfsTer19
ENST00000680783.1:c.521_522insAGGCTGTACAGGG ENSP00000506329.1:p.Leu175GlyfsTer19
ENST00000681269.1:c.521_522insAGGCTGTACAGGG ENSP00000505985.1:p.Leu175GlyfsTer19
ENST00000681347.1:n.1032_1033insAGGCTGTACAGGG
ENST00000681514.1:c.521_522insAGGCTGTACAGGG ENSP00000505963.1:p.Leu175GlyfsTer19
ENST00000681772.1:c.521_522insAGGCTGTACAGGG ENSP00000505829.1:p.Leu175GlyfsTer19
ENST00000366667.4:c.548_549insAGGCTGTACAGGG ENSP00000355627.4:p.Leu184GlyfsTer19
NM_000029.3:c.548_549insAGGCTGTACAGGG NP_000020.1:p.Leu184GlyfsTer19
NM_000029.4:c.548_549insAGGCTGTACAGGG NP_000020.1:p.Leu184GlyfsTer19
NM_001382817.3:c.521_522insAGGCTGTACAGGG NP_001369746.2:p.Leu175GlyfsTer19
NM_001384479.1:c.521_522insAGGCTGTACAGGG MANE Select NP_001371408.1:p.Leu175GlyfsTer19