Canonical Allele Identifier: CA402158236
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598632A>C , CM000680.2:g.31598632A>C GRCh38
NC_000018.9:g.29178595A>C , CM000680.1:g.29178595A>C GRCh37
NC_000018.8:g.27432593A>C NCBI36
NG_009490.1:g.11866A>C , LRG_416:g.11866A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.401A>C MANE Select ENSP00000237014.4:p.Tyr134Ser
ENST00000610404.5:c.305A>C ENSP00000477599.2:p.Tyr102Ser
ENST00000649620.1:c.401A>C ENSP00000497927.1:p.Tyr134Ser
ENST00000237014.7:c.401A>C ENSP00000237014.3:p.Tyr134Ser
ENST00000610404.4:c.515A>C ENSP00000477599.1:p.Tyr172Ser
ENST00000613781.1:c.377A>C ENSP00000479174.1:p.Tyr126Ser
NM_000371.3:c.401A>C , LRG_416t1:c.401A>C NP_000362.1:p.Tyr134Ser
NM_000371.4:c.401A>C MANE Select NP_000362.1:p.Tyr134Ser