Canonical Allele Identifier: CA2293886865

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31593025G= , CM000680.2:g.31593025G=	GRCh38
NC_000018.9:g.29172988G= , CM000680.1:g.29172988G=	GRCh37
NC_000018.8:g.27426986G=	NCBI36
NG_009490.1:g.6259G= , LRG_416:g.6259G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.199G= MANE Select	ENSP00000237014.4:p.Gly67=
ENST00000610404.5:c.103G=	ENSP00000477599.2:p.Gly35=
ENST00000649620.1:c.199G=	ENSP00000497927.1:p.Gly67=
ENST00000237014.7:c.199G=	ENSP00000237014.3:p.Gly67=
ENST00000432547.7:n.225G=
ENST00000541025.2:n.225G=
ENST00000610404.4:c.199G=	ENSP00000477599.1:p.Gly67=
ENST00000613781.1:c.199G=	ENSP00000479174.1:p.Gly67=
NM_000371.3:c.199G= , LRG_416t1:c.199G=	NP_000362.1:p.Gly67=
NM_000371.4:c.199G= MANE Select	NP_000362.1:p.Gly67=