Canonical Allele Identifier: CA2293889351

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31598613G= , CM000680.2:g.31598613G=	GRCh38
NC_000018.9:g.29178576G= , CM000680.1:g.29178576G=	GRCh37
NC_000018.8:g.27432574G=	NCBI36
NG_009490.1:g.11847G= , LRG_416:g.11847G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000237014.8:c.382G= MANE Select	ENSP00000237014.4:p.Ala128=
ENST00000610404.5:c.286G=	ENSP00000477599.2:p.Ala96=
ENST00000649620.1:c.382G=	ENSP00000497927.1:p.Ala128=
ENST00000237014.7:c.382G=	ENSP00000237014.3:p.Ala128=
ENST00000610404.4:c.496G=	ENSP00000477599.1:p.Ala166=
ENST00000613781.1:c.375+7G=	ENSP00000479174.1:n.375+7G=
NM_000371.3:c.382G= , LRG_416t1:c.382G=	NP_000362.1:p.Ala128=
NM_000371.4:c.382G= MANE Select	NP_000362.1:p.Ala128=