Canonical Allele Identifier: CA8928369

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31591888C>T , CM000680.2:g.31591888C>T	GRCh38
NC_000018.9:g.29171851C>T , CM000680.1:g.29171851C>T	GRCh37
NC_000018.8:g.27425849C>T	NCBI36
NG_009490.1:g.5122C>T , LRG_416:g.5122C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000371.4:c.-15C>T MANE Select	NP_000362.1:n.-15C>T
ENST00000237014.8:c.-15C>T MANE Select	ENSP00000237014.4:n.-15C>T
NM_000371.3:c.-15C>T , LRG_416t1:c.-15C>T	NP_000362.1:n.-15C>T
ENST00000237014.7:c.-15C>T	ENSP00000237014.3:n.-15C>T
ENST00000432547.7:n.12C>T
ENST00000541025.2:n.12C>T
ENST00000610404.4:c.-15C>T	ENSP00000477599.1:n.-15C>T
ENST00000610404.5:c.-27-1008C>T	ENSP00000477599.2:n.-27-1008C>T
ENST00000613781.1:c.-15C>T	ENSP00000479174.1:n.-15C>T
ENST00000613781.2:c.-1-14C>T	ENSP00000479174.2:n.-1-14C>T
ENST00000649620.1:c.-1-14C>T	ENSP00000497927.1:n.-1-14C>T
ENST00000676075.1:c.-1-14C>T	ENSP00000502027.1:n.-1-14C>T