Canonical Allele Identifier: CA1779607974
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838837_42838838delinsGA , CM000670.2:g.42838837_42838838delinsGA GRCh38
NC_000008.10:g.42693980_42693981delinsGA , CM000670.1:g.42693980_42693981delinsGA GRCh37
NC_000008.9:g.42813137_42813138delinsGA NCBI36
NG_011837.1:g.9494_9495delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+348_267+349delinsTC MANE Select ENSP00000254250.3:n.267+348_267+349delinsTC
ENST00000345117.2:c.72-502_72-501delinsTC ENSP00000344966.2:n.72-502_72-501delinsTC
ENST00000529779.1:c.267+348_267+349delinsTC ENSP00000433912.1:n.267+348_267+349delinsTC
NM_018105.2:c.267+348_267+349delinsTC NP_060575.1:n.267+348_267+349delinsTC
NM_199003.1:c.72-502_72-501delinsTC NP_945354.1:n.72-502_72-501delinsTC
NM_018105.3:c.267+348_267+349delinsTC MANE Select NP_060575.1:n.267+348_267+349delinsTC
NM_199003.2:c.72-502_72-501delinsTC NP_945354.1:n.72-502_72-501delinsTC