Canonical Allele Identifier: CA629154715
Gene: TTR HGNC NCBI

Linked Data

dbSNP Id: rs1226138545
gnomAD v2: 18-29175010-TG-T
gnomAD v3: 18-31595047-TG-T
gnomAD v4: 18-31595047-TG-T
MyVariant Identifiers: chr18:g.29175011del (hg19) chr18:g.31595048del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31595052del , CM000680.2:g.31595052del GRCh38
NC_000018.9:g.29175015del , CM000680.1:g.29175015del GRCh37
NC_000018.8:g.27429013del NCBI36
NG_009490.1:g.8286del , LRG_416:g.8286del

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.201-68del MANE Select ENSP00000237014.4:n.201-68del
ENST00000610404.5:c.105-68del ENSP00000477599.2:n.105-68del
ENST00000649620.1:c.201-68del ENSP00000497927.1:n.201-68del
ENST00000237014.7:c.201-68del ENSP00000237014.3:n.201-68del
ENST00000541025.2:n.227-68del
ENST00000610404.4:c.201-68del ENSP00000477599.1:n.201-68del
ENST00000613781.1:c.201-68del ENSP00000479174.1:n.201-68del
NM_000371.3:c.201-68del , LRG_416t1:c.201-68del NP_000362.1:n.201-68del
NM_000371.4:c.201-68del MANE Select NP_000362.1:n.201-68del
Search 100 bp 5'
Search 100 bp 3'