Canonical Allele Identifier: CA402156902

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595124A>T , CM000680.2:g.31595124A>T	GRCh38
NC_000018.9:g.29175087A>T , CM000680.1:g.29175087A>T	GRCh37
NC_000018.8:g.27429085A>T	NCBI36
NG_009490.1:g.8358A>T , LRG_416:g.8358A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000371.4:c.205A>T MANE Select	NP_000362.1:p.Thr69Ser
ENST00000237014.8:c.205A>T MANE Select	ENSP00000237014.4:p.Thr69Ser
NM_000371.3:c.205A>T , LRG_416t1:c.205A>T	NP_000362.1:p.Thr69Ser
ENST00000237014.7:c.205A>T	ENSP00000237014.3:p.Thr69Ser
ENST00000541025.2:n.231A>T
ENST00000610404.4:c.205A>T	ENSP00000477599.1:p.Thr69Ser
ENST00000610404.5:c.109A>T	ENSP00000477599.2:p.Thr37Ser
ENST00000613781.1:c.205A>T	ENSP00000479174.1:p.Thr69Ser
ENST00000649620.1:c.205A>T	ENSP00000497927.1:p.Thr69Ser