Canonical Allele Identifier: CA2293889408
Gene: TTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598709G= , CM000680.2:g.31598709G= GRCh38
NC_000018.9:g.29178672G= , CM000680.1:g.29178672G= GRCh37
NC_000018.8:g.27432670G= NCBI36
NG_009490.1:g.11943G= , LRG_416:g.11943G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.*34G= MANE Select ENSP00000237014.4:n.*34G=
ENST00000610404.5:c.*34G= ENSP00000477599.2:n.*34G=
ENST00000649620.1:c.*34G= ENSP00000497927.1:n.*34G=
ENST00000237014.7:c.*34G= ENSP00000237014.3:n.*34G=
ENST00000610404.4:c.*34G= ENSP00000477599.1:n.*34G=
NM_000371.3:c.*34G= , LRG_416t1:c.*34G= NP_000362.1:n.*34G=
NM_000371.4:c.*34G= MANE Select NP_000362.1:n.*34G=
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