Canonical Allele Identifier: CA778418508

Gene: TTR

Linked Data

• dbSNP Id: rs1486158132
• MyVariant Identifiers: chr18:g.29178637del (hg19) ; chr18:g.31598674del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598674del , CM000680.2:g.31598674del	GRCh38
NC_000018.9:g.29178637del , CM000680.1:g.29178637del	GRCh37
NC_000018.8:g.27432635del	NCBI36
NG_009490.1:g.11908del , LRG_416:g.11908del

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.443del MANE Select	ENSP00000237014.4:p.Ter148=
ENST00000610404.5:c.347del	ENSP00000477599.2:p.Ter116=
ENST00000649620.1:c.443del	ENSP00000497927.1:p.Ter148=
ENST00000237014.7:c.443del	ENSP00000237014.3:p.Ter148=
ENST00000610404.4:c.557del	ENSP00000477599.1:p.Ter186=
ENST00000613781.1:c.419del	ENSP00000479174.1:p.Ter140=
NM_000371.3:c.443del , LRG_416t1:c.443del	NP_000362.1:p.Ter148=
NM_000371.4:c.443del MANE Select	NP_000362.1:p.Ter148=