Canonical Allele Identifier: CA2812000706
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598505_31598513dup , CM000680.2:g.31598505_31598513dup GRCh38
NC_000018.9:g.29178468_29178476dup , CM000680.1:g.29178468_29178476dup GRCh37
NC_000018.8:g.27432466_27432474dup NCBI36
NG_009490.1:g.11739_11747dup , LRG_416:g.11739_11747dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000237014.8:c.337-63_337-55dup MANE Select ENSP00000237014.4:n.337-63_337-55dup
ENST00000610404.5:c.241-63_241-55dup ENSP00000477599.2:n.241-63_241-55dup
ENST00000649620.1:c.337-63_337-55dup ENSP00000497927.1:n.337-63_337-55dup
ENST00000237014.7:c.337-63_337-55dup ENSP00000237014.3:n.337-63_337-55dup
ENST00000610404.4:c.451-63_451-55dup ENSP00000477599.1:n.451-63_451-55dup
ENST00000613781.1:c.337-63_337-55dup ENSP00000479174.1:n.337-63_337-55dup
NM_000371.3:c.337-63_337-55dup , LRG_416t1:c.337-63_337-55dup NP_000362.1:n.337-63_337-55dup
NM_000371.4:c.337-63_337-55dup MANE Select NP_000362.1:n.337-63_337-55dup