Canonical Allele Identifier: CA2293889368

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598642C= , CM000680.2:g.31598642C=	GRCh38
NC_000018.9:g.29178605C= , CM000680.1:g.29178605C=	GRCh37
NC_000018.8:g.27432603C=	NCBI36
NG_009490.1:g.11876C= , LRG_416:g.11876C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.411C= MANE Select	ENSP00000237014.4:p.Ser137=
ENST00000610404.5:c.315C=	ENSP00000477599.2:p.Ser105=
ENST00000649620.1:c.411C=	ENSP00000497927.1:p.Ser137=
ENST00000237014.7:c.411C=	ENSP00000237014.3:p.Ser137=
ENST00000610404.4:c.525C=	ENSP00000477599.1:p.Ser175=
ENST00000613781.1:c.387C=	ENSP00000479174.1:p.Ser129=
NM_000371.3:c.411C= , LRG_416t1:c.411C=	NP_000362.1:p.Ser137=
NM_000371.4:c.411C= MANE Select	NP_000362.1:p.Ser137=