Canonical Allele Identifier: CA402158125
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598572T>A , CM000680.2:g.31598572T>A GRCh38
NC_000018.9:g.29178535T>A , CM000680.1:g.29178535T>A GRCh37
NC_000018.8:g.27432533T>A NCBI36
NG_009490.1:g.11806T>A , LRG_416:g.11806T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.341T>A MANE Select ENSP00000237014.4:p.Val114Glu
ENST00000610404.5:c.245T>A ENSP00000477599.2:p.Val82Glu
ENST00000649620.1:c.341T>A ENSP00000497927.1:p.Val114Glu
ENST00000237014.7:c.341T>A ENSP00000237014.3:p.Val114Glu
ENST00000610404.4:c.455T>A ENSP00000477599.1:p.Val152Glu
ENST00000613781.1:c.341T>A ENSP00000479174.1:p.Val114Glu
NM_000371.3:c.341T>A , LRG_416t1:c.341T>A NP_000362.1:p.Val114Glu
NM_000371.4:c.341T>A MANE Select NP_000362.1:p.Val114Glu