Canonical Allele Identifier: CA2293886586
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592413G= , CM000680.2:g.31592413G= GRCh38
NC_000018.9:g.29172376G= , CM000680.1:g.29172376G= GRCh37
NC_000018.8:g.27426374G= NCBI36
NG_009490.1:g.5647G= , LRG_416:g.5647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.69+442G= MANE Select ENSP00000237014.4:n.69+442G=
ENST00000610404.5:c.-27-483G= ENSP00000477599.2:n.-27-483G=
ENST00000649620.1:c.69+442G= ENSP00000497927.1:n.69+442G=
ENST00000237014.7:c.69+442G= ENSP00000237014.3:n.69+442G=
ENST00000432547.7:n.95+442G=
ENST00000541025.2:n.95+442G=
ENST00000610404.4:c.69+442G= ENSP00000477599.1:n.69+442G=
ENST00000613781.1:c.69+442G= ENSP00000479174.1:n.69+442G=
NM_000371.3:c.69+442G= , LRG_416t1:c.69+442G= NP_000362.1:n.69+442G=
NM_000371.4:c.69+442G= MANE Select NP_000362.1:n.69+442G=