Canonical Allele Identifier: CA2293889321
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598565T= , CM000680.2:g.31598565T= GRCh38
NC_000018.9:g.29178528T= , CM000680.1:g.29178528T= GRCh37
NC_000018.8:g.27432526T= NCBI36
NG_009490.1:g.11799T= , LRG_416:g.11799T=

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-3T= MANE Select ENSP00000237014.4:n.337-3T=
ENST00000610404.5:c.241-3T= ENSP00000477599.2:n.241-3T=
ENST00000649620.1:c.337-3T= ENSP00000497927.1:n.337-3T=
ENST00000237014.7:c.337-3T= ENSP00000237014.3:n.337-3T=
ENST00000610404.4:c.451-3T= ENSP00000477599.1:n.451-3T=
ENST00000613781.1:c.337-3T= ENSP00000479174.1:n.337-3T=
NM_000371.3:c.337-3T= , LRG_416t1:c.337-3T= NP_000362.1:n.337-3T=
NM_000371.4:c.337-3T= MANE Select NP_000362.1:n.337-3T=