Canonical Allele Identifier: CA371107659
Gene: THAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839188T>G , CM000670.2:g.42839188T>G GRCh38
NC_000008.10:g.42694331T>G , CM000670.1:g.42694331T>G GRCh37
NC_000008.9:g.42813488T>G NCBI36
NG_011837.1:g.9144A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.265A>C MANE Select ENSP00000254250.3:p.Lys89Gln
ENST00000345117.2:c.72-852A>C ENSP00000344966.2:n.72-852A>C
ENST00000529779.1:c.265A>C ENSP00000433912.1:p.Lys89Gln
NM_018105.2:c.265A>C NP_060575.1:p.Lys89Gln
NM_199003.1:c.72-852A>C NP_945354.1:n.72-852A>C
NM_018105.3:c.265A>C MANE Select NP_060575.1:p.Lys89Gln
NM_199003.2:c.72-852A>C NP_945354.1:n.72-852A>C