Canonical Allele Identifier: CA1779610123
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843045T= , CM000670.2:g.42843045T= GRCh38
NC_000008.10:g.42698188T= , CM000670.1:g.42698188T= GRCh37
NC_000008.9:g.42817345T= NCBI36
NG_011837.1:g.5287A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.50A= MANE Select ENSP00000254250.3:p.Asp17=
ENST00000345117.2:c.50A= ENSP00000344966.2:p.Asp17=
ENST00000529779.1:c.50A= ENSP00000433912.1:p.Asp17=
NM_018105.2:c.50A= NP_060575.1:p.Asp17=
NM_199003.1:c.50A= NP_945354.1:p.Asp17=
NM_018105.3:c.50A= MANE Select NP_060575.1:p.Asp17=
NM_199003.2:c.50A= NP_945354.1:p.Asp17=