Canonical Allele Identifier: CA2739580362
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598534T>C , CM000680.2:g.31598534T>C GRCh38
NC_000018.9:g.29178497T>C , CM000680.1:g.29178497T>C GRCh37
NC_000018.8:g.27432495T>C NCBI36
NG_009490.1:g.11768T>C , LRG_416:g.11768T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-34T>C MANE Select ENSP00000237014.4:n.337-34T>C
ENST00000610404.5:c.241-34T>C ENSP00000477599.2:n.241-34T>C
ENST00000649620.1:c.337-34T>C ENSP00000497927.1:n.337-34T>C
ENST00000237014.7:c.337-34T>C ENSP00000237014.3:n.337-34T>C
ENST00000610404.4:c.451-34T>C ENSP00000477599.1:n.451-34T>C
ENST00000613781.1:c.337-34T>C ENSP00000479174.1:n.337-34T>C
NM_000371.3:c.337-34T>C , LRG_416t1:c.337-34T>C NP_000362.1:n.337-34T>C
NM_000371.4:c.337-34T>C MANE Select NP_000362.1:n.337-34T>C