Canonical Allele Identifier: CA1779607937
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838763_42838764delinsTA , CM000670.2:g.42838763_42838764delinsTA GRCh38
NC_000008.10:g.42693906_42693907delinsTA , CM000670.1:g.42693906_42693907delinsTA GRCh37
NC_000008.9:g.42813063_42813064delinsTA NCBI36
NG_011837.1:g.9568_9569delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+422_267+423delinsTA MANE Select ENSP00000254250.3:n.267+422_267+423delinsTA
ENST00000345117.2:c.72-428_72-427delinsTA ENSP00000344966.2:n.72-428_72-427delinsTA
ENST00000529779.1:c.267+422_267+423delinsTA ENSP00000433912.1:n.267+422_267+423delinsTA
NM_018105.2:c.267+422_267+423delinsTA NP_060575.1:n.267+422_267+423delinsTA
NM_199003.1:c.72-428_72-427delinsTA NP_945354.1:n.72-428_72-427delinsTA
NM_018105.3:c.267+422_267+423delinsTA MANE Select NP_060575.1:n.267+422_267+423delinsTA
NM_199003.2:c.72-428_72-427delinsTA NP_945354.1:n.72-428_72-427delinsTA