Canonical Allele Identifier: CA2565012467
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598539G>T , CM000680.2:g.31598539G>T GRCh38
NC_000018.9:g.29178502G>T , CM000680.1:g.29178502G>T GRCh37
NC_000018.8:g.27432500G>T NCBI36
NG_009490.1:g.11773G>T , LRG_416:g.11773G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-29G>T MANE Select ENSP00000237014.4:n.337-29G>T
ENST00000610404.5:c.241-29G>T ENSP00000477599.2:n.241-29G>T
ENST00000649620.1:c.337-29G>T ENSP00000497927.1:n.337-29G>T
ENST00000237014.7:c.337-29G>T ENSP00000237014.3:n.337-29G>T
ENST00000610404.4:c.451-29G>T ENSP00000477599.1:n.451-29G>T
ENST00000613781.1:c.337-29G>T ENSP00000479174.1:n.337-29G>T
NM_000371.3:c.337-29G>T , LRG_416t1:c.337-29G>T NP_000362.1:n.337-29G>T
NM_000371.4:c.337-29G>T MANE Select NP_000362.1:n.337-29G>T