Canonical Allele Identifier: CA2293889362
Gene: TTR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.401A= MANE Select ENSP00000237014.4:p.Tyr134=
ENST00000610404.5:c.305A= ENSP00000477599.2:p.Tyr102=
ENST00000649620.1:c.401A= ENSP00000497927.1:p.Tyr134=
ENST00000237014.7:c.401A= ENSP00000237014.3:p.Tyr134=
ENST00000610404.4:c.515A= ENSP00000477599.1:p.Tyr172=
ENST00000613781.1:c.377A= ENSP00000479174.1:p.Tyr126=
NM_000371.3:c.401A= , LRG_416t1:c.401A= NP_000362.1:p.Tyr134=
NM_000371.4:c.401A= MANE Select NP_000362.1:p.Tyr134=