Canonical Allele Identifier: CA402156839

Gene: TTR

Linked Data

• MyVariant Identifiers: chr18:g.29172965A>T (hg19) ; chr18:g.31593002A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31593002A>T , CM000680.2:g.31593002A>T	GRCh38
NC_000018.9:g.29172965A>T , CM000680.1:g.29172965A>T	GRCh37
NC_000018.8:g.27426963A>T	NCBI36
NG_009490.1:g.6236A>T , LRG_416:g.6236A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.176A>T MANE Select	ENSP00000237014.4:p.Asp59Val
ENST00000610404.5:c.80A>T	ENSP00000477599.2:p.Asp27Val
ENST00000649620.1:c.176A>T	ENSP00000497927.1:p.Asp59Val
ENST00000237014.7:c.176A>T	ENSP00000237014.3:p.Asp59Val
ENST00000432547.7:n.202A>T
ENST00000541025.2:n.202A>T
ENST00000610404.4:c.176A>T	ENSP00000477599.1:p.Asp59Val
ENST00000613781.1:c.176A>T	ENSP00000479174.1:p.Asp59Val
NM_000371.3:c.176A>T , LRG_416t1:c.176A>T	NP_000362.1:p.Asp59Val
NM_000371.4:c.176A>T MANE Select	NP_000362.1:p.Asp59Val