Canonical Allele Identifier: CA2293889384

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598671A= , CM000680.2:g.31598671A=	GRCh38
NC_000018.9:g.29178634A= , CM000680.1:g.29178634A=	GRCh37
NC_000018.8:g.27432632A=	NCBI36
NG_009490.1:g.11905A= , LRG_416:g.11905A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.440A= MANE Select	ENSP00000237014.4:p.Glu147=
ENST00000610404.5:c.344A=	ENSP00000477599.2:p.Glu115=
ENST00000649620.1:c.440A=	ENSP00000497927.1:p.Glu147=
ENST00000237014.7:c.440A=	ENSP00000237014.3:p.Glu147=
ENST00000610404.4:c.554A=	ENSP00000477599.1:p.Glu185=
ENST00000613781.1:c.416A=	ENSP00000479174.1:p.Glu139=
NM_000371.3:c.440A= , LRG_416t1:c.440A=	NP_000362.1:p.Glu147=
NM_000371.4:c.440A= MANE Select	NP_000362.1:p.Glu147=