Canonical Allele Identifier: CA2293887764

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595070C= , CM000680.2:g.31595070C=	GRCh38
NC_000018.9:g.29175033C= , CM000680.1:g.29175033C=	GRCh37
NC_000018.8:g.27429031C=	NCBI36
NG_009490.1:g.8304C= , LRG_416:g.8304C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.201-50C= MANE Select	ENSP00000237014.4:n.201-50C=
ENST00000610404.5:c.105-50C=	ENSP00000477599.2:n.105-50C=
ENST00000649620.1:c.201-50C=	ENSP00000497927.1:n.201-50C=
ENST00000237014.7:c.201-50C=	ENSP00000237014.3:n.201-50C=
ENST00000541025.2:n.227-50C=
ENST00000610404.4:c.201-50C=	ENSP00000477599.1:n.201-50C=
ENST00000613781.1:c.201-50C=	ENSP00000479174.1:n.201-50C=
NM_000371.3:c.201-50C= , LRG_416t1:c.201-50C=	NP_000362.1:n.201-50C=
NM_000371.4:c.201-50C= MANE Select	NP_000362.1:n.201-50C=