Canonical Allele Identifier: CA2293887726

Gene: TTR

Linked Data

• dbSNP Id: rs2073509174

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31594984dup , CM000680.2:g.31594984dup	GRCh38
NC_000018.9:g.29174947dup , CM000680.1:g.29174947dup	GRCh37
NC_000018.8:g.27428945dup	NCBI36
NG_009490.1:g.8218dup , LRG_416:g.8218dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.201-136dup MANE Select	ENSP00000237014.4:n.201-136dup
ENST00000610404.5:c.105-136dup	ENSP00000477599.2:n.105-136dup
ENST00000649620.1:c.201-136dup	ENSP00000497927.1:n.201-136dup
ENST00000237014.7:c.201-136dup	ENSP00000237014.3:n.201-136dup
ENST00000541025.2:n.227-136dup
ENST00000610404.4:c.201-136dup	ENSP00000477599.1:n.201-136dup
ENST00000613781.1:c.201-136dup	ENSP00000479174.1:n.201-136dup
NM_000371.3:c.201-136dup , LRG_416t1:c.201-136dup	NP_000362.1:n.201-136dup
NM_000371.4:c.201-136dup MANE Select	NP_000362.1:n.201-136dup