Canonical Allele Identifier: CA2293886883

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31593053G= , CM000680.2:g.31593053G=	GRCh38
NC_000018.9:g.29173016G= , CM000680.1:g.29173016G=	GRCh37
NC_000018.8:g.27427014G=	NCBI36
NG_009490.1:g.6287G= , LRG_416:g.6287G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.200+27G= MANE Select	ENSP00000237014.4:n.200+27G=
ENST00000610404.5:c.104+27G=	ENSP00000477599.2:n.104+27G=
ENST00000649620.1:c.200+27G=	ENSP00000497927.1:n.200+27G=
ENST00000237014.7:c.200+27G=	ENSP00000237014.3:n.200+27G=
ENST00000432547.7:n.253G=
ENST00000541025.2:n.226+27G=
ENST00000610404.4:c.200+27G=	ENSP00000477599.1:n.200+27G=
ENST00000613781.1:c.200+27G=	ENSP00000479174.1:n.200+27G=
NM_000371.3:c.200+27G= , LRG_416t1:c.200+27G=	NP_000362.1:n.200+27G=
NM_000371.4:c.200+27G= MANE Select	NP_000362.1:n.200+27G=