Canonical Allele Identifier: CA1779608122
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839194G= , CM000670.2:g.42839194G= GRCh38
NC_000008.10:g.42694337G= , CM000670.1:g.42694337G= GRCh37
NC_000008.9:g.42813494G= NCBI36
NG_011837.1:g.9138C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.259C= MANE Select ENSP00000254250.3:p.His87=
ENST00000345117.2:c.72-858C= ENSP00000344966.2:n.72-858C=
ENST00000529779.1:c.259C= ENSP00000433912.1:p.His87=
NM_018105.2:c.259C= NP_060575.1:p.His87=
NM_199003.1:c.72-858C= NP_945354.1:n.72-858C=
NM_018105.3:c.259C= MANE Select NP_060575.1:p.His87=
NM_199003.2:c.72-858C= NP_945354.1:n.72-858C=