Canonical Allele Identifier: CA2739580352
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598525T>A , CM000680.2:g.31598525T>A GRCh38
NC_000018.9:g.29178488T>A , CM000680.1:g.29178488T>A GRCh37
NC_000018.8:g.27432486T>A NCBI36
NG_009490.1:g.11759T>A , LRG_416:g.11759T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.337-43T>A MANE Select ENSP00000237014.4:n.337-43T>A
ENST00000610404.5:c.241-43T>A ENSP00000477599.2:n.241-43T>A
ENST00000649620.1:c.337-43T>A ENSP00000497927.1:n.337-43T>A
ENST00000237014.7:c.337-43T>A ENSP00000237014.3:n.337-43T>A
ENST00000610404.4:c.451-43T>A ENSP00000477599.1:n.451-43T>A
ENST00000613781.1:c.337-43T>A ENSP00000479174.1:n.337-43T>A
NM_000371.3:c.337-43T>A , LRG_416t1:c.337-43T>A NP_000362.1:n.337-43T>A
NM_000371.4:c.337-43T>A MANE Select NP_000362.1:n.337-43T>A