Canonical Allele Identifier: CA2499307109
Gene: TTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31598648_31598652delinsCAA , CM000680.2:g.31598648_31598652delinsCAA GRCh38
NC_000018.9:g.29178611_29178615delinsCAA , CM000680.1:g.29178611_29178615delinsCAA GRCh37
NC_000018.8:g.27432609_27432613delinsCAA NCBI36
NG_009490.1:g.11882_11886delinsCAA , LRG_416:g.11882_11886delinsCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000237014.8:c.417_421delinsCAA MANE Select ENSP00000237014.4:p.Ala140AsnfsTer?
ENST00000610404.5:c.321_325delinsCAA ENSP00000477599.2:p.Ala108AsnfsTer?
ENST00000649620.1:c.417_421delinsCAA ENSP00000497927.1:p.Ala140AsnfsTer?
ENST00000237014.7:c.417_421delinsCAA ENSP00000237014.3:p.Ala140AsnfsTer?
ENST00000610404.4:c.531_535delinsCAA ENSP00000477599.1:p.Ala178AsnfsTer?
ENST00000613781.1:c.393_397delinsCAA ENSP00000479174.1:p.Ala132AsnfsTer?
NM_000371.3:c.417_421delinsCAA , LRG_416t1:c.417_421delinsCAA NP_000362.1:p.Ala140AsnfsTer?
NM_000371.4:c.417_421delinsCAA MANE Select NP_000362.1:p.Ala140AsnfsTer?