Canonical Allele Identifier: CA2293886767
Gene: TTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592852C= , CM000680.2:g.31592852C= GRCh38
NC_000018.9:g.29172815C= , CM000680.1:g.29172815C= GRCh37
NC_000018.8:g.27426813C= NCBI36
NG_009490.1:g.6086C= , LRG_416:g.6086C=

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.70-44C= MANE Select ENSP00000237014.4:n.70-44C=
ENST00000610404.5:c.-27-44C= ENSP00000477599.2:n.-27-44C=
ENST00000649620.1:c.70-44C= ENSP00000497927.1:n.70-44C=
ENST00000237014.7:c.70-44C= ENSP00000237014.3:n.70-44C=
ENST00000432547.7:n.96-44C=
ENST00000541025.2:n.96-44C=
ENST00000610404.4:c.70-44C= ENSP00000477599.1:n.70-44C=
ENST00000613781.1:c.70-44C= ENSP00000479174.1:n.70-44C=
NM_000371.3:c.70-44C= , LRG_416t1:c.70-44C= NP_000362.1:n.70-44C=
NM_000371.4:c.70-44C= MANE Select NP_000362.1:n.70-44C=
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