Canonical Allele Identifier: CA8928511
Gene: TTR HGNC NCBI

Linked Data

dbSNP Id: rs777190076

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598640T>A , CM000680.2:g.31598640T>A GRCh38
NC_000018.9:g.29178603T>A , CM000680.1:g.29178603T>A GRCh37
NC_000018.8:g.27432601T>A NCBI36
NG_009490.1:g.11874T>A , LRG_416:g.11874T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.409T>A MANE Select ENSP00000237014.4:p.Ser137Thr
ENST00000610404.5:c.313T>A ENSP00000477599.2:p.Ser105Thr
ENST00000649620.1:c.409T>A ENSP00000497927.1:p.Ser137Thr
ENST00000237014.7:c.409T>A ENSP00000237014.3:p.Ser137Thr
ENST00000610404.4:c.523T>A ENSP00000477599.1:p.Ser175Thr
ENST00000613781.1:c.385T>A ENSP00000479174.1:p.Ser129Thr
NM_000371.3:c.409T>A , LRG_416t1:c.409T>A NP_000362.1:p.Ser137Thr
NM_000371.4:c.409T>A MANE Select NP_000362.1:p.Ser137Thr