Canonical Allele Identifier: CA402158238
Gene: TTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598633C>G , CM000680.2:g.31598633C>G GRCh38
NC_000018.9:g.29178596C>G , CM000680.1:g.29178596C>G GRCh37
NC_000018.8:g.27432594C>G NCBI36
NG_009490.1:g.11867C>G , LRG_416:g.11867C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.402C>G MANE Select ENSP00000237014.4:p.Tyr134Ter
ENST00000610404.5:c.306C>G ENSP00000477599.2:p.Tyr102Ter
ENST00000649620.1:c.402C>G ENSP00000497927.1:p.Tyr134Ter
ENST00000237014.7:c.402C>G ENSP00000237014.3:p.Tyr134Ter
ENST00000610404.4:c.516C>G ENSP00000477599.1:p.Tyr172Ter
ENST00000613781.1:c.378C>G ENSP00000479174.1:p.Tyr126Ter
NM_000371.3:c.402C>G , LRG_416t1:c.402C>G NP_000362.1:p.Tyr134Ter
NM_000371.4:c.402C>G MANE Select NP_000362.1:p.Tyr134Ter