Canonical Allele Identifier: CA371107704
Gene: THAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1586456954

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839211A>C , CM000670.2:g.42839211A>C GRCh38
NC_000008.10:g.42694354A>C , CM000670.1:g.42694354A>C GRCh37
NC_000008.9:g.42813511A>C NCBI36
NG_011837.1:g.9121T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.242T>G MANE Select ENSP00000254250.3:p.Phe81Cys
ENST00000345117.2:c.72-875T>G ENSP00000344966.2:n.72-875T>G
ENST00000529779.1:c.242T>G ENSP00000433912.1:p.Phe81Cys
ENST00000532093.1:n.472T>G
NM_018105.2:c.242T>G NP_060575.1:p.Phe81Cys
NM_199003.1:c.72-875T>G NP_945354.1:n.72-875T>G
NM_018105.3:c.242T>G MANE Select NP_060575.1:p.Phe81Cys
NM_199003.2:c.72-875T>G NP_945354.1:n.72-875T>G