Canonical Allele Identifier: CA1779608121
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839193T= , CM000670.2:g.42839193T= GRCh38
NC_000008.10:g.42694336T= , CM000670.1:g.42694336T= GRCh37
NC_000008.9:g.42813493T= NCBI36
NG_011837.1:g.9139A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.260A= MANE Select ENSP00000254250.3:p.His87=
ENST00000345117.2:c.72-857A= ENSP00000344966.2:n.72-857A=
ENST00000529779.1:c.260A= ENSP00000433912.1:p.His87=
NM_018105.2:c.260A= NP_060575.1:p.His87=
NM_199003.1:c.72-857A= NP_945354.1:n.72-857A=
NM_018105.3:c.260A= MANE Select NP_060575.1:p.His87=
NM_199003.2:c.72-857A= NP_945354.1:n.72-857A=