Canonical Allele Identifier: CA2293889377
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598658_31598664delinsACCAATC , CM000680.2:g.31598658_31598664delinsACCAATC GRCh38
NC_000018.9:g.29178621_29178627delinsACCAATC , CM000680.1:g.29178621_29178627delinsACCAATC GRCh37
NC_000018.8:g.27432619_27432625delinsACCAATC NCBI36
NG_009490.1:g.11892_11898delinsACCAATC , LRG_416:g.11892_11898delinsACCAATC

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.427_433delinsACCAATC MANE Select ENSP00000237014.4:p.Thr143=
ENST00000610404.5:c.331_337delinsACCAATC ENSP00000477599.2:p.Thr111=
ENST00000649620.1:c.427_433delinsACCAATC ENSP00000497927.1:p.Thr143=
ENST00000237014.7:c.427_433delinsACCAATC ENSP00000237014.3:p.Thr143=
ENST00000610404.4:c.541_547delinsACCAATC ENSP00000477599.1:p.Thr181=
ENST00000613781.1:c.403_409delinsACCAATC ENSP00000479174.1:p.Thr135=
NM_000371.3:c.427_433delinsACCAATC , LRG_416t1:c.427_433delinsACCAATC NP_000362.1:p.Thr143=
NM_000371.4:c.427_433delinsACCAATC MANE Select NP_000362.1:p.Thr143=