Canonical Allele Identifier: CA2293886882
Gene: TTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31593051C= , CM000680.2:g.31593051C= GRCh38
NC_000018.9:g.29173014C= , CM000680.1:g.29173014C= GRCh37
NC_000018.8:g.27427012C= NCBI36
NG_009490.1:g.6285C= , LRG_416:g.6285C=

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.200+25C= MANE Select ENSP00000237014.4:n.200+25C=
ENST00000610404.5:c.104+25C= ENSP00000477599.2:n.104+25C=
ENST00000649620.1:c.200+25C= ENSP00000497927.1:n.200+25C=
ENST00000237014.7:c.200+25C= ENSP00000237014.3:n.200+25C=
ENST00000432547.7:n.251C=
ENST00000541025.2:n.226+25C=
ENST00000610404.4:c.200+25C= ENSP00000477599.1:n.200+25C=
ENST00000613781.1:c.200+25C= ENSP00000479174.1:n.200+25C=
NM_000371.3:c.200+25C= , LRG_416t1:c.200+25C= NP_000362.1:n.200+25C=
NM_000371.4:c.200+25C= MANE Select NP_000362.1:n.200+25C=
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