Canonical Allele Identifier: CA402157140
Gene: TTR HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31595244G>A , CM000680.2:g.31595244G>A GRCh38
NC_000018.9:g.29175207G>A , CM000680.1:g.29175207G>A GRCh37
NC_000018.8:g.27429205G>A NCBI36
NG_009490.1:g.8478G>A , LRG_416:g.8478G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.325G>A MANE Select ENSP00000237014.4:p.Glu109Lys
ENST00000610404.5:c.229G>A ENSP00000477599.2:p.Glu77Lys
ENST00000649620.1:c.325G>A ENSP00000497927.1:p.Glu109Lys
ENST00000237014.7:c.325G>A ENSP00000237014.3:p.Glu109Lys
ENST00000541025.2:n.351G>A
ENST00000610404.4:c.325G>A ENSP00000477599.1:p.Glu109Lys
ENST00000613781.1:c.325G>A ENSP00000479174.1:p.Glu109Lys
NM_000371.3:c.325G>A , LRG_416t1:c.325G>A NP_000362.1:p.Glu109Lys
NM_000371.4:c.325G>A MANE Select NP_000362.1:p.Glu109Lys