Canonical Allele Identifier: CA1779607954
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838792_42838794delinsTCA , CM000670.2:g.42838792_42838794delinsTCA GRCh38
NC_000008.10:g.42693935_42693937delinsTCA , CM000670.1:g.42693935_42693937delinsTCA GRCh37
NC_000008.9:g.42813092_42813094delinsTCA NCBI36
NG_011837.1:g.9538_9540delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+392_267+394delinsTGA MANE Select ENSP00000254250.3:n.267+392_267+394delinsTGA
ENST00000345117.2:c.72-458_72-456delinsTGA ENSP00000344966.2:n.72-458_72-456delinsTGA
ENST00000529779.1:c.267+392_267+394delinsTGA ENSP00000433912.1:n.267+392_267+394delinsTGA
NM_018105.2:c.267+392_267+394delinsTGA NP_060575.1:n.267+392_267+394delinsTGA
NM_199003.1:c.72-458_72-456delinsTGA NP_945354.1:n.72-458_72-456delinsTGA
NM_018105.3:c.267+392_267+394delinsTGA MANE Select NP_060575.1:n.267+392_267+394delinsTGA
NM_199003.2:c.72-458_72-456delinsTGA NP_945354.1:n.72-458_72-456delinsTGA