Canonical Allele Identifier: CA1779607953
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838791T= , CM000670.2:g.42838791T= GRCh38
NC_000008.10:g.42693934T= , CM000670.1:g.42693934T= GRCh37
NC_000008.9:g.42813091T= NCBI36
NG_011837.1:g.9541A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+395A= MANE Select ENSP00000254250.3:n.267+395A=
ENST00000345117.2:c.72-455A= ENSP00000344966.2:n.72-455A=
ENST00000529779.1:c.267+395A= ENSP00000433912.1:n.267+395A=
NM_018105.2:c.267+395A= NP_060575.1:n.267+395A=
NM_199003.1:c.72-455A= NP_945354.1:n.72-455A=
NM_018105.3:c.267+395A= MANE Select NP_060575.1:n.267+395A=
NM_199003.2:c.72-455A= NP_945354.1:n.72-455A=