Canonical Allele Identifier: CA778414778

Gene: TTR

Linked Data

• dbSNP Id: rs1260706055
• gnomAD v4: 18-31592813-TC-T
• MyVariant Identifiers: chr18:g.29172777del (hg19) ; chr18:g.31592814del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592815del , CM000680.2:g.31592815del	GRCh38
NC_000018.9:g.29172778del , CM000680.1:g.29172778del	GRCh37
NC_000018.8:g.27426776del	NCBI36
NG_009490.1:g.6049del , LRG_416:g.6049del

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.70-81del MANE Select	ENSP00000237014.4:n.70-81del
ENST00000610404.5:c.-27-81del	ENSP00000477599.2:n.-27-81del
ENST00000649620.1:c.70-81del	ENSP00000497927.1:n.70-81del
ENST00000237014.7:c.70-81del	ENSP00000237014.3:n.70-81del
ENST00000432547.7:n.96-81del
ENST00000541025.2:n.96-81del
ENST00000610404.4:c.70-81del	ENSP00000477599.1:n.70-81del
ENST00000613781.1:c.70-81del	ENSP00000479174.1:n.70-81del
NM_000371.3:c.70-81del , LRG_416t1:c.70-81del	NP_000362.1:n.70-81del
NM_000371.4:c.70-81del MANE Select	NP_000362.1:n.70-81del