Canonical Allele Identifier: CA2293887904

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595345G= , CM000680.2:g.31595345G=	GRCh38
NC_000018.9:g.29175308G= , CM000680.1:g.29175308G=	GRCh37
NC_000018.8:g.27429306G=	NCBI36
NG_009490.1:g.8579G= , LRG_416:g.8579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.336+90G= MANE Select	ENSP00000237014.4:n.336+90G=
ENST00000610404.5:c.240+90G=	ENSP00000477599.2:n.240+90G=
ENST00000649620.1:c.336+90G=	ENSP00000497927.1:n.336+90G=
ENST00000237014.7:c.336+90G=	ENSP00000237014.3:n.336+90G=
ENST00000541025.2:n.452G=
ENST00000610404.4:c.357+69G=	ENSP00000477599.1:n.357+69G=
ENST00000613781.1:c.336+90G=	ENSP00000479174.1:n.336+90G=
NM_000371.3:c.336+90G= , LRG_416t1:c.336+90G=	NP_000362.1:n.336+90G=
NM_000371.4:c.336+90G= MANE Select	NP_000362.1:n.336+90G=