Canonical Allele Identifier: CA402158268
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598649G>C , CM000680.2:g.31598649G>C GRCh38
NC_000018.9:g.29178612G>C , CM000680.1:g.29178612G>C GRCh37
NC_000018.8:g.27432610G>C NCBI36
NG_009490.1:g.11883G>C , LRG_416:g.11883G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.418G>C MANE Select ENSP00000237014.4:p.Ala140Pro
ENST00000610404.5:c.322G>C ENSP00000477599.2:p.Ala108Pro
ENST00000649620.1:c.418G>C ENSP00000497927.1:p.Ala140Pro
ENST00000237014.7:c.418G>C ENSP00000237014.3:p.Ala140Pro
ENST00000610404.4:c.532G>C ENSP00000477599.1:p.Ala178Pro
ENST00000613781.1:c.394G>C ENSP00000479174.1:p.Ala132Pro
NM_000371.3:c.418G>C , LRG_416t1:c.418G>C NP_000362.1:p.Ala140Pro
NM_000371.4:c.418G>C MANE Select NP_000362.1:p.Ala140Pro