Canonical Allele Identifier: CA916081932
Gene: TTR HGNC NCBI

Linked Data

ClinVar Variation Id: 842048
ClinVar RCV Id: RCV001044394
dbSNP Id: rs2073525314

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598041_31598580del , CM000680.2:g.31598041_31598580del GRCh38
NC_000018.9:g.29178004_29178543del , CM000680.1:g.29178004_29178543del GRCh37
NC_000018.8:g.27432002_27432541del NCBI36
NG_009490.1:g.11275_11814del , LRG_416:g.11275_11814del

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.337-527_349del
ENST00000610404.5:c.241-527_253del
ENST00000649620.1:c.337-527_349del
ENST00000237014.7:c.337-527_349del
ENST00000610404.4:c.431-32_463del
ENST00000613781.1:c.337-527_349del
NM_000371.3:c.337-527_349del , LRG_416t1:c.337-527_349del
NM_000371.4:c.337-527_349del