Canonical Allele Identifier: CA2293886864

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31593021C= , CM000680.2:g.31593021C=	GRCh38
NC_000018.9:g.29172984C= , CM000680.1:g.29172984C=	GRCh37
NC_000018.8:g.27426982C=	NCBI36
NG_009490.1:g.6255C= , LRG_416:g.6255C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.195C= MANE Select	ENSP00000237014.4:p.Ala65=
ENST00000610404.5:c.99C=	ENSP00000477599.2:p.Ala33=
ENST00000649620.1:c.195C=	ENSP00000497927.1:p.Ala65=
ENST00000237014.7:c.195C=	ENSP00000237014.3:p.Ala65=
ENST00000432547.7:n.221C=
ENST00000541025.2:n.221C=
ENST00000610404.4:c.195C=	ENSP00000477599.1:p.Ala65=
ENST00000613781.1:c.195C=	ENSP00000479174.1:p.Ala65=
NM_000371.3:c.195C= , LRG_416t1:c.195C=	NP_000362.1:p.Ala65=
NM_000371.4:c.195C= MANE Select	NP_000362.1:p.Ala65=