Canonical Allele Identifier: CA2293886749
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592813T= , CM000680.2:g.31592813T= GRCh38
NC_000018.9:g.29172776T= , CM000680.1:g.29172776T= GRCh37
NC_000018.8:g.27426774T= NCBI36
NG_009490.1:g.6047T= , LRG_416:g.6047T=

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.70-83T= MANE Select ENSP00000237014.4:n.70-83T=
ENST00000610404.5:c.-27-83T= ENSP00000477599.2:n.-27-83T=
ENST00000649620.1:c.70-83T= ENSP00000497927.1:n.70-83T=
ENST00000237014.7:c.70-83T= ENSP00000237014.3:n.70-83T=
ENST00000432547.7:n.96-83T=
ENST00000541025.2:n.96-83T=
ENST00000610404.4:c.70-83T= ENSP00000477599.1:n.70-83T=
ENST00000613781.1:c.70-83T= ENSP00000479174.1:n.70-83T=
NM_000371.3:c.70-83T= , LRG_416t1:c.70-83T= NP_000362.1:n.70-83T=
NM_000371.4:c.70-83T= MANE Select NP_000362.1:n.70-83T=