Canonical Allele Identifier: CA2293887914

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595377A= , CM000680.2:g.31595377A=	GRCh38
NC_000018.9:g.29175340A= , CM000680.1:g.29175340A=	GRCh37
NC_000018.8:g.27429338A=	NCBI36
NG_009490.1:g.8611A= , LRG_416:g.8611A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+122A= MANE Select	ENSP00000237014.4:n.336+122A=
ENST00000610404.5:c.240+122A=	ENSP00000477599.2:n.240+122A=
ENST00000649620.1:c.336+122A=	ENSP00000497927.1:n.336+122A=
ENST00000237014.7:c.336+122A=	ENSP00000237014.3:n.336+122A=
ENST00000541025.2:n.484A=
ENST00000610404.4:c.357+101A=	ENSP00000477599.1:n.357+101A=
ENST00000613781.1:c.336+122A=	ENSP00000479174.1:n.336+122A=
NM_000371.3:c.336+122A= , LRG_416t1:c.336+122A=	NP_000362.1:n.336+122A=
NM_000371.4:c.336+122A= MANE Select	NP_000362.1:n.336+122A=