Canonical Allele Identifier: CA402157002

Gene: TTR

Linked Data

• ClinVar Variation Id: 935886
• ClinVar RCV Id: RCV001204571
• dbSNP Id: rs2073510816
• MyVariant Identifiers: chr18:g.29175140A>T (hg19) ; chr18:g.31595177A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31595177A>T , CM000680.2:g.31595177A>T	GRCh38
NC_000018.9:g.29175140A>T , CM000680.1:g.29175140A>T	GRCh37
NC_000018.8:g.27429138A>T	NCBI36
NG_009490.1:g.8411A>T , LRG_416:g.8411A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.258A>T MANE Select	ENSP00000237014.4:p.Glu86Asp
ENST00000610404.5:c.162A>T	ENSP00000477599.2:p.Glu54Asp
ENST00000649620.1:c.258A>T	ENSP00000497927.1:p.Glu86Asp
ENST00000237014.7:c.258A>T	ENSP00000237014.3:p.Glu86Asp
ENST00000541025.2:n.284A>T
ENST00000610404.4:c.258A>T	ENSP00000477599.1:p.Glu86Asp
ENST00000613781.1:c.258A>T	ENSP00000479174.1:p.Glu86Asp
NM_000371.3:c.258A>T , LRG_416t1:c.258A>T	NP_000362.1:p.Glu86Asp
NM_000371.4:c.258A>T MANE Select	NP_000362.1:p.Glu86Asp