Canonical Allele Identifier: CA2293886796

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592914T= , CM000680.2:g.31592914T=	GRCh38
NC_000018.9:g.29172877T= , CM000680.1:g.29172877T=	GRCh37
NC_000018.8:g.27426875T=	NCBI36
NG_009490.1:g.6148T= , LRG_416:g.6148T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.88T= MANE Select	ENSP00000237014.4:p.Cys30=
ENST00000610404.5:c.-9T=	ENSP00000477599.2:n.-9T=
ENST00000649620.1:c.88T=	ENSP00000497927.1:p.Cys30=
ENST00000237014.7:c.88T=	ENSP00000237014.3:p.Cys30=
ENST00000432547.7:n.114T=
ENST00000541025.2:n.114T=
ENST00000610404.4:c.88T=	ENSP00000477599.1:p.Cys30=
ENST00000613781.1:c.88T=	ENSP00000479174.1:p.Cys30=
NM_000371.3:c.88T= , LRG_416t1:c.88T=	NP_000362.1:p.Cys30=
NM_000371.4:c.88T= MANE Select	NP_000362.1:p.Cys30=