Canonical Allele Identifier: CA2739580364
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598536G>C , CM000680.2:g.31598536G>C GRCh38
NC_000018.9:g.29178499G>C , CM000680.1:g.29178499G>C GRCh37
NC_000018.8:g.27432497G>C NCBI36
NG_009490.1:g.11770G>C , LRG_416:g.11770G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-32G>C MANE Select ENSP00000237014.4:n.337-32G>C
ENST00000610404.5:c.241-32G>C ENSP00000477599.2:n.241-32G>C
ENST00000649620.1:c.337-32G>C ENSP00000497927.1:n.337-32G>C
ENST00000237014.7:c.337-32G>C ENSP00000237014.3:n.337-32G>C
ENST00000610404.4:c.451-32G>C ENSP00000477599.1:n.451-32G>C
ENST00000613781.1:c.337-32G>C ENSP00000479174.1:n.337-32G>C
NM_000371.3:c.337-32G>C , LRG_416t1:c.337-32G>C NP_000362.1:n.337-32G>C
NM_000371.4:c.337-32G>C MANE Select NP_000362.1:n.337-32G>C