Canonical Allele Identifier: CA1779607921
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838735_42838739delinsTACTG , CM000670.2:g.42838735_42838739delinsTACTG GRCh38
NC_000008.10:g.42693878_42693882delinsTACTG , CM000670.1:g.42693878_42693882delinsTACTG GRCh37
NC_000008.9:g.42813035_42813039delinsTACTG NCBI36
NG_011837.1:g.9593_9597delinsCAGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.268-403_268-399delinsCAGTA MANE Select ENSP00000254250.3:n.268-403_268-399delinsCAGTA
ENST00000345117.2:c.72-403_72-399delinsCAGTA ENSP00000344966.2:n.72-403_72-399delinsCAGTA
ENST00000529779.1:c.267+447_267+451delinsCAGTA ENSP00000433912.1:n.267+447_267+451delinsCAGTA
NM_018105.2:c.268-403_268-399delinsCAGTA NP_060575.1:n.268-403_268-399delinsCAGTA
NM_199003.1:c.72-403_72-399delinsCAGTA NP_945354.1:n.72-403_72-399delinsCAGTA
NM_018105.3:c.268-403_268-399delinsCAGTA MANE Select NP_060575.1:n.268-403_268-399delinsCAGTA
NM_199003.2:c.72-403_72-399delinsCAGTA NP_945354.1:n.72-403_72-399delinsCAGTA