Canonical Allele Identifier: CA2739580273
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31595319T>A , CM000680.2:g.31595319T>A GRCh38
NC_000018.9:g.29175282T>A , CM000680.1:g.29175282T>A GRCh37
NC_000018.8:g.27429280T>A NCBI36
NG_009490.1:g.8553T>A , LRG_416:g.8553T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.336+64T>A MANE Select ENSP00000237014.4:n.336+64T>A
ENST00000610404.5:c.240+64T>A ENSP00000477599.2:n.240+64T>A
ENST00000649620.1:c.336+64T>A ENSP00000497927.1:n.336+64T>A
ENST00000237014.7:c.336+64T>A ENSP00000237014.3:n.336+64T>A
ENST00000541025.2:n.426T>A
ENST00000610404.4:c.357+43T>A ENSP00000477599.1:n.357+43T>A
ENST00000613781.1:c.336+64T>A ENSP00000479174.1:n.336+64T>A
NM_000371.3:c.336+64T>A , LRG_416t1:c.336+64T>A NP_000362.1:n.336+64T>A
NM_000371.4:c.336+64T>A MANE Select NP_000362.1:n.336+64T>A