Canonical Allele Identifier: CA1779607958
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838802T= , CM000670.2:g.42838802T= GRCh38
NC_000008.10:g.42693945T= , CM000670.1:g.42693945T= GRCh37
NC_000008.9:g.42813102T= NCBI36
NG_011837.1:g.9530A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+384A= MANE Select ENSP00000254250.3:n.267+384A=
ENST00000345117.2:c.72-466A= ENSP00000344966.2:n.72-466A=
ENST00000529779.1:c.267+384A= ENSP00000433912.1:n.267+384A=
NM_018105.2:c.267+384A= NP_060575.1:n.267+384A=
NM_199003.1:c.72-466A= NP_945354.1:n.72-466A=
NM_018105.3:c.267+384A= MANE Select NP_060575.1:n.267+384A=
NM_199003.2:c.72-466A= NP_945354.1:n.72-466A=