Canonical Allele Identifier: CA8928372

Gene: TTR

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31591900A>G , CM000680.2:g.31591900A>G	GRCh38
NC_000018.9:g.29171863A>G , CM000680.1:g.29171863A>G	GRCh37
NC_000018.8:g.27425861A>G	NCBI36
NG_009490.1:g.5134A>G , LRG_416:g.5134A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000371.4:c.-3A>G MANE Select	NP_000362.1:n.-3A>G
ENST00000237014.8:c.-3A>G MANE Select	ENSP00000237014.4:n.-3A>G
NM_000371.3:c.-3A>G , LRG_416t1:c.-3A>G	NP_000362.1:n.-3A>G
ENST00000237014.7:c.-3A>G	ENSP00000237014.3:n.-3A>G
ENST00000432547.7:n.24A>G
ENST00000541025.2:n.24A>G
ENST00000610404.4:c.-3A>G	ENSP00000477599.1:n.-3A>G
ENST00000610404.5:c.-27-996A>G	ENSP00000477599.2:n.-27-996A>G
ENST00000613781.1:c.-3A>G	ENSP00000479174.1:n.-3A>G
ENST00000613781.2:c.-1-2A>G	ENSP00000479174.2:n.-1-2A>G
ENST00000649620.1:c.-1-2A>G	ENSP00000497927.1:n.-1-2A>G
ENST00000676075.1:c.-1-2A>G	ENSP00000502027.1:n.-1-2A>G