Canonical Allele Identifier: CA2293886737
Gene: TTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31592793G= , CM000680.2:g.31592793G= GRCh38
NC_000018.9:g.29172756G= , CM000680.1:g.29172756G= GRCh37
NC_000018.8:g.27426754G= NCBI36
NG_009490.1:g.6027G= , LRG_416:g.6027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.70-103G= MANE Select ENSP00000237014.4:n.70-103G=
ENST00000610404.5:c.-27-103G= ENSP00000477599.2:n.-27-103G=
ENST00000649620.1:c.70-103G= ENSP00000497927.1:n.70-103G=
ENST00000237014.7:c.70-103G= ENSP00000237014.3:n.70-103G=
ENST00000432547.7:n.96-103G=
ENST00000541025.2:n.96-103G=
ENST00000610404.4:c.70-103G= ENSP00000477599.1:n.70-103G=
ENST00000613781.1:c.70-103G= ENSP00000479174.1:n.70-103G=
NM_000371.3:c.70-103G= , LRG_416t1:c.70-103G= NP_000362.1:n.70-103G=
NM_000371.4:c.70-103G= MANE Select NP_000362.1:n.70-103G=
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