Canonical Allele Identifier: CA402158139

Gene: TTR

Linked Data

• MyVariant Identifiers: chr18:g.29178540A>G (hg19) ; chr18:g.31598577A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598577A>G , CM000680.2:g.31598577A>G	GRCh38
NC_000018.9:g.29178540A>G , CM000680.1:g.29178540A>G	GRCh37
NC_000018.8:g.27432538A>G	NCBI36
NG_009490.1:g.11811A>G , LRG_416:g.11811A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.346A>G MANE Select	ENSP00000237014.4:p.Thr116Ala
ENST00000610404.5:c.250A>G	ENSP00000477599.2:p.Thr84Ala
ENST00000649620.1:c.346A>G	ENSP00000497927.1:p.Thr116Ala
ENST00000237014.7:c.346A>G	ENSP00000237014.3:p.Thr116Ala
ENST00000610404.4:c.460A>G	ENSP00000477599.1:p.Thr154Ala
ENST00000613781.1:c.346A>G	ENSP00000479174.1:p.Thr116Ala
NM_000371.3:c.346A>G , LRG_416t1:c.346A>G	NP_000362.1:p.Thr116Ala
NM_000371.4:c.346A>G MANE Select	NP_000362.1:p.Thr116Ala