Canonical Allele Identifier: CA503610173

Gene: TTR

Linked Data

• MyVariant Identifiers: chr18:g.29172969C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31593006C>A , CM000680.2:g.31593006C>A	GRCh38
NC_000018.9:g.29172969C>A , CM000680.1:g.29172969C>A	GRCh37
NC_000018.8:g.27426967C>A	NCBI36
NG_009490.1:g.6240C>A , LRG_416:g.6240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000237014.8:c.180C>A MANE Select	ENSP00000237014.4:p.Thr60=
ENST00000610404.5:c.84C>A	ENSP00000477599.2:p.Thr28=
ENST00000649620.1:c.180C>A	ENSP00000497927.1:p.Thr60=
ENST00000237014.7:c.180C>A	ENSP00000237014.3:p.Thr60=
ENST00000432547.7:n.206C>A
ENST00000541025.2:n.206C>A
ENST00000610404.4:c.180C>A	ENSP00000477599.1:p.Thr60=
ENST00000613781.1:c.180C>A	ENSP00000479174.1:p.Thr60=
NM_000371.3:c.180C>A , LRG_416t1:c.180C>A	NP_000362.1:p.Thr60=
NM_000371.4:c.180C>A MANE Select	NP_000362.1:p.Thr60=