Canonical Allele Identifier: CA2739268809
Gene: TTPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2813619
ClinVar RCV Id: RCV003680533

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63073002del , CM000670.2:g.63073002del GRCh38
NC_000008.10:g.63985561del , CM000670.1:g.63985561del GRCh37
NC_000008.9:g.64148115del NCBI36
NG_016123.1:g.18053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260116.5:c.292del MANE Select ENSP00000260116.4:p.Ala98LeufsTer7
ENST00000260116.4:c.292del ENSP00000260116.4:p.Ala98LeufsTer7
ENST00000521138.1:n.232+12817del
NM_000370.3:c.292del MANE Select NP_000361.1:p.Ala98LeufsTer7
XM_006716468.2:c.205-8685del XP_006716531.1:n.205-8685del
XM_006716468.4:c.205-8685del XP_006716531.1:n.205-8685del