Canonical Allele Identifier: CA2717208500
Gene: THAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2128918546

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838751G>T , CM000670.2:g.42838751G>T GRCh38
NC_000008.10:g.42693894G>T , CM000670.1:g.42693894G>T GRCh37
NC_000008.9:g.42813051G>T NCBI36
NG_011837.1:g.9581C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.268-415C>A MANE Select ENSP00000254250.3:n.268-415C>A
ENST00000345117.2:c.72-415C>A ENSP00000344966.2:n.72-415C>A
ENST00000529779.1:c.267+435C>A ENSP00000433912.1:n.267+435C>A
NM_018105.2:c.268-415C>A NP_060575.1:n.268-415C>A
NM_199003.1:c.72-415C>A NP_945354.1:n.72-415C>A
NM_018105.3:c.268-415C>A MANE Select NP_060575.1:n.268-415C>A
NM_199003.2:c.72-415C>A NP_945354.1:n.72-415C>A