Canonical Allele Identifier: CA402158242
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598634T>G , CM000680.2:g.31598634T>G GRCh38
NC_000018.9:g.29178597T>G , CM000680.1:g.29178597T>G GRCh37
NC_000018.8:g.27432595T>G NCBI36
NG_009490.1:g.11868T>G , LRG_416:g.11868T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.403T>G MANE Select ENSP00000237014.4:p.Ser135Ala
ENST00000610404.5:c.307T>G ENSP00000477599.2:p.Ser103Ala
ENST00000649620.1:c.403T>G ENSP00000497927.1:p.Ser135Ala
ENST00000237014.7:c.403T>G ENSP00000237014.3:p.Ser135Ala
ENST00000610404.4:c.517T>G ENSP00000477599.1:p.Ser173Ala
ENST00000613781.1:c.379T>G ENSP00000479174.1:p.Ser127Ala
NM_000371.3:c.403T>G , LRG_416t1:c.403T>G NP_000362.1:p.Ser135Ala
NM_000371.4:c.403T>G MANE Select NP_000362.1:p.Ser135Ala