Canonical Allele Identifier: CA371107716
Gene: THAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839217G>C , CM000670.2:g.42839217G>C GRCh38
NC_000008.10:g.42694360G>C , CM000670.1:g.42694360G>C GRCh37
NC_000008.9:g.42813517G>C NCBI36
NG_011837.1:g.9115C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.236C>G MANE Select ENSP00000254250.3:p.Thr79Arg
ENST00000345117.2:c.72-881C>G ENSP00000344966.2:n.72-881C>G
ENST00000529779.1:c.236C>G ENSP00000433912.1:p.Thr79Arg
ENST00000532093.1:n.466C>G
NM_018105.2:c.236C>G NP_060575.1:p.Thr79Arg
NM_199003.1:c.72-881C>G NP_945354.1:n.72-881C>G
NM_018105.3:c.236C>G MANE Select NP_060575.1:p.Thr79Arg
NM_199003.2:c.72-881C>G NP_945354.1:n.72-881C>G