Canonical Allele Identifier: CA402158270
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598650C>G , CM000680.2:g.31598650C>G GRCh38
NC_000018.9:g.29178613C>G , CM000680.1:g.29178613C>G GRCh37
NC_000018.8:g.27432611C>G NCBI36
NG_009490.1:g.11884C>G , LRG_416:g.11884C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.419C>G MANE Select ENSP00000237014.4:p.Ala140Gly
ENST00000610404.5:c.323C>G ENSP00000477599.2:p.Ala108Gly
ENST00000649620.1:c.419C>G ENSP00000497927.1:p.Ala140Gly
ENST00000237014.7:c.419C>G ENSP00000237014.3:p.Ala140Gly
ENST00000610404.4:c.533C>G ENSP00000477599.1:p.Ala178Gly
ENST00000613781.1:c.395C>G ENSP00000479174.1:p.Ala132Gly
NM_000371.3:c.419C>G , LRG_416t1:c.419C>G NP_000362.1:p.Ala140Gly
NM_000371.4:c.419C>G MANE Select NP_000362.1:p.Ala140Gly