Canonical Allele Identifier: CA1779607968
Gene: THAP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838821_42838825delinsTAGAG , CM000670.2:g.42838821_42838825delinsTAGAG GRCh38
NC_000008.10:g.42693964_42693968delinsTAGAG , CM000670.1:g.42693964_42693968delinsTAGAG GRCh37
NC_000008.9:g.42813121_42813125delinsTAGAG NCBI36
NG_011837.1:g.9507_9511delinsCTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+361_267+365delinsCTCTA MANE Select ENSP00000254250.3:n.267+361_267+365delinsCTCTA
ENST00000345117.2:c.72-489_72-485delinsCTCTA ENSP00000344966.2:n.72-489_72-485delinsCTCTA
ENST00000529779.1:c.267+361_267+365delinsCTCTA ENSP00000433912.1:n.267+361_267+365delinsCTCTA
NM_018105.2:c.267+361_267+365delinsCTCTA NP_060575.1:n.267+361_267+365delinsCTCTA
NM_199003.1:c.72-489_72-485delinsCTCTA NP_945354.1:n.72-489_72-485delinsCTCTA
NM_018105.3:c.267+361_267+365delinsCTCTA MANE Select NP_060575.1:n.267+361_267+365delinsCTCTA
NM_199003.2:c.72-489_72-485delinsCTCTA NP_945354.1:n.72-489_72-485delinsCTCTA
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