Canonical Allele Identifier: CA1779608040
Gene: THAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838980G= , CM000670.2:g.42838980G= GRCh38
NC_000008.10:g.42694123G= , CM000670.1:g.42694123G= GRCh37
NC_000008.9:g.42813280G= NCBI36
NG_011837.1:g.9352C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+206C= MANE Select ENSP00000254250.3:n.267+206C=
ENST00000345117.2:c.72-644C= ENSP00000344966.2:n.72-644C=
ENST00000529779.1:c.267+206C= ENSP00000433912.1:n.267+206C=
NM_018105.2:c.267+206C= NP_060575.1:n.267+206C=
NM_199003.1:c.72-644C= NP_945354.1:n.72-644C=
NM_018105.3:c.267+206C= MANE Select NP_060575.1:n.267+206C=
NM_199003.2:c.72-644C= NP_945354.1:n.72-644C=