Canonical Allele Identifier: CA1779610118
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843034A= , CM000670.2:g.42843034A= GRCh38
NC_000008.10:g.42698177A= , CM000670.1:g.42698177A= GRCh37
NC_000008.9:g.42817334A= NCBI36
NG_011837.1:g.5298T=

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.61T= MANE Select ENSP00000254250.3:p.Ser21=
ENST00000345117.2:c.61T= ENSP00000344966.2:p.Ser21=
ENST00000529779.1:c.61T= ENSP00000433912.1:p.Ser21=
NM_018105.2:c.61T= NP_060575.1:p.Ser21=
NM_199003.1:c.61T= NP_945354.1:p.Ser21=
NM_018105.3:c.61T= MANE Select NP_060575.1:p.Ser21=
NM_199003.2:c.61T= NP_945354.1:p.Ser21=