Canonical Allele Identifier: CA2293886592

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592417T= , CM000680.2:g.31592417T=	GRCh38
NC_000018.9:g.29172380T= , CM000680.1:g.29172380T=	GRCh37
NC_000018.8:g.27426378T=	NCBI36
NG_009490.1:g.5651T= , LRG_416:g.5651T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.69+446T= MANE Select	ENSP00000237014.4:n.69+446T=
ENST00000610404.5:c.-27-479T=	ENSP00000477599.2:n.-27-479T=
ENST00000649620.1:c.69+446T=	ENSP00000497927.1:n.69+446T=
ENST00000237014.7:c.69+446T=	ENSP00000237014.3:n.69+446T=
ENST00000432547.7:n.95+446T=
ENST00000541025.2:n.95+446T=
ENST00000610404.4:c.69+446T=	ENSP00000477599.1:n.69+446T=
ENST00000613781.1:c.69+446T=	ENSP00000479174.1:n.69+446T=
NM_000371.3:c.69+446T= , LRG_416t1:c.69+446T=	NP_000362.1:n.69+446T=
NM_000371.4:c.69+446T= MANE Select	NP_000362.1:n.69+446T=