Canonical Allele Identifier: CA2293889298
Gene: TTR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598529G= , CM000680.2:g.31598529G= GRCh38
NC_000018.9:g.29178492G= , CM000680.1:g.29178492G= GRCh37
NC_000018.8:g.27432490G= NCBI36
NG_009490.1:g.11763G= , LRG_416:g.11763G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.337-39G= MANE Select ENSP00000237014.4:n.337-39G=
ENST00000610404.5:c.241-39G= ENSP00000477599.2:n.241-39G=
ENST00000649620.1:c.337-39G= ENSP00000497927.1:n.337-39G=
ENST00000237014.7:c.337-39G= ENSP00000237014.3:n.337-39G=
ENST00000610404.4:c.451-39G= ENSP00000477599.1:n.451-39G=
ENST00000613781.1:c.337-39G= ENSP00000479174.1:n.337-39G=
NM_000371.3:c.337-39G= , LRG_416t1:c.337-39G= NP_000362.1:n.337-39G=
NM_000371.4:c.337-39G= MANE Select NP_000362.1:n.337-39G=
Search 100 bp 5'
Search 100 bp 3'