Canonical Allele Identifier: CA2293889363

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598636C= , CM000680.2:g.31598636C=	GRCh38
NC_000018.9:g.29178599C= , CM000680.1:g.29178599C=	GRCh37
NC_000018.8:g.27432597C=	NCBI36
NG_009490.1:g.11870C= , LRG_416:g.11870C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.405C= MANE Select	ENSP00000237014.4:p.Ser135=
ENST00000610404.5:c.309C=	ENSP00000477599.2:p.Ser103=
ENST00000649620.1:c.405C=	ENSP00000497927.1:p.Ser135=
ENST00000237014.7:c.405C=	ENSP00000237014.3:p.Ser135=
ENST00000610404.4:c.519C=	ENSP00000477599.1:p.Ser173=
ENST00000613781.1:c.381C=	ENSP00000479174.1:p.Ser127=
NM_000371.3:c.405C= , LRG_416t1:c.405C=	NP_000362.1:p.Ser135=
NM_000371.4:c.405C= MANE Select	NP_000362.1:p.Ser135=