Canonical Allele Identifier: CA402156671
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592956C>G , CM000680.2:g.31592956C>G GRCh38
NC_000018.9:g.29172919C>G , CM000680.1:g.29172919C>G GRCh37
NC_000018.8:g.27426917C>G NCBI36
NG_009490.1:g.6190C>G , LRG_416:g.6190C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.130C>G MANE Select ENSP00000237014.4:p.Pro44Ala
ENST00000610404.5:c.34C>G ENSP00000477599.2:p.Pro12Ala
ENST00000649620.1:c.130C>G ENSP00000497927.1:p.Pro44Ala
ENST00000237014.7:c.130C>G ENSP00000237014.3:p.Pro44Ala
ENST00000432547.7:n.156C>G
ENST00000541025.2:n.156C>G
ENST00000610404.4:c.130C>G ENSP00000477599.1:p.Pro44Ala
ENST00000613781.1:c.130C>G ENSP00000479174.1:p.Pro44Ala
NM_000371.3:c.130C>G , LRG_416t1:c.130C>G NP_000362.1:p.Pro44Ala
NM_000371.4:c.130C>G MANE Select NP_000362.1:p.Pro44Ala