Canonical Allele Identifier: CA2293886803

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31592937A= , CM000680.2:g.31592937A=	GRCh38
NC_000018.9:g.29172900A= , CM000680.1:g.29172900A=	GRCh37
NC_000018.8:g.27426898A=	NCBI36
NG_009490.1:g.6171A= , LRG_416:g.6171A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.111A= MANE Select	ENSP00000237014.4:p.Leu37=
ENST00000610404.5:c.15A=	ENSP00000477599.2:p.Leu5=
ENST00000649620.1:c.111A=	ENSP00000497927.1:p.Leu37=
ENST00000237014.7:c.111A=	ENSP00000237014.3:p.Leu37=
ENST00000432547.7:n.137A=
ENST00000541025.2:n.137A=
ENST00000610404.4:c.111A=	ENSP00000477599.1:p.Leu37=
ENST00000613781.1:c.111A=	ENSP00000479174.1:p.Leu37=
NM_000371.3:c.111A= , LRG_416t1:c.111A=	NP_000362.1:p.Leu37=
NM_000371.4:c.111A= MANE Select	NP_000362.1:p.Leu37=