Canonical Allele Identifier: CA2839596261

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598686C>A , CM000680.2:g.31598686C>A	GRCh38
NC_000018.9:g.29178649C>A , CM000680.1:g.29178649C>A	GRCh37
NC_000018.8:g.27432647C>A	NCBI36
NG_009490.1:g.11920C>A , LRG_416:g.11920C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.*11C>A MANE Select	ENSP00000237014.4:n.*11C>A
ENST00000610404.5:c.*11C>A	ENSP00000477599.2:n.*11C>A
ENST00000649620.1:c.*11C>A	ENSP00000497927.1:n.*11C>A
ENST00000237014.7:c.*11C>A	ENSP00000237014.3:n.*11C>A
ENST00000610404.4:c.*11C>A	ENSP00000477599.1:n.*11C>A
NM_000371.3:c.*11C>A , LRG_416t1:c.*11C>A	NP_000362.1:n.*11C>A
NM_000371.4:c.*11C>A MANE Select	NP_000362.1:n.*11C>A