Canonical Allele Identifier: CA2687441772
Gene: TTPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.63072896del , CM000670.2:g.63072896del GRCh38
NC_000008.10:g.63985455del , CM000670.1:g.63985455del GRCh37
NC_000008.9:g.64148009del NCBI36
NG_016123.1:g.18159del

Transcript Alleles

HGVS Amino-acid change
ENST00000260116.5:c.358+40del MANE Select ENSP00000260116.4:n.358+40del
ENST00000260116.4:c.358+40del ENSP00000260116.4:n.358+40del
ENST00000521138.1:n.232+12923del
NM_000370.3:c.358+40del MANE Select NP_000361.1:n.358+40del
XM_006716468.2:c.205-8579del XP_006716531.1:n.205-8579del
XM_006716468.4:c.205-8579del XP_006716531.1:n.205-8579del