Canonical Allele Identifier: CA2293887787

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595125C= , CM000680.2:g.31595125C=	GRCh38
NC_000018.9:g.29175088C= , CM000680.1:g.29175088C=	GRCh37
NC_000018.8:g.27429086C=	NCBI36
NG_009490.1:g.8359C= , LRG_416:g.8359C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.206C= MANE Select	ENSP00000237014.4:p.Thr69=
ENST00000610404.5:c.110C=	ENSP00000477599.2:p.Thr37=
ENST00000649620.1:c.206C=	ENSP00000497927.1:p.Thr69=
ENST00000237014.7:c.206C=	ENSP00000237014.3:p.Thr69=
ENST00000541025.2:n.232C=
ENST00000610404.4:c.206C=	ENSP00000477599.1:p.Thr69=
ENST00000613781.1:c.206C=	ENSP00000479174.1:p.Thr69=
NM_000371.3:c.206C= , LRG_416t1:c.206C=	NP_000362.1:p.Thr69=
NM_000371.4:c.206C= MANE Select	NP_000362.1:p.Thr69=