Canonical Allele Identifier: CA2293886802

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592934T= , CM000680.2:g.31592934T=	GRCh38
NC_000018.9:g.29172897T= , CM000680.1:g.29172897T=	GRCh37
NC_000018.8:g.27426895T=	NCBI36
NG_009490.1:g.6168T= , LRG_416:g.6168T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.108T= MANE Select	ENSP00000237014.4:p.Val36=
ENST00000610404.5:c.12T=	ENSP00000477599.2:p.Val4=
ENST00000649620.1:c.108T=	ENSP00000497927.1:p.Val36=
ENST00000237014.7:c.108T=	ENSP00000237014.3:p.Val36=
ENST00000432547.7:n.134T=
ENST00000541025.2:n.134T=
ENST00000610404.4:c.108T=	ENSP00000477599.1:p.Val36=
ENST00000613781.1:c.108T=	ENSP00000479174.1:p.Val36=
NM_000371.3:c.108T= , LRG_416t1:c.108T=	NP_000362.1:p.Val36=
NM_000371.4:c.108T= MANE Select	NP_000362.1:p.Val36=