Canonical Allele Identifier: CA460569210
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42698181G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843038G>C , CM000670.2:g.42843038G>C GRCh38
NC_000008.10:g.42698181G>C , CM000670.1:g.42698181G>C GRCh37
NC_000008.9:g.42817338G>C NCBI36
NG_011837.1:g.5294C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.57C>G MANE Select ENSP00000254250.3:p.Pro19=
ENST00000345117.2:c.57C>G ENSP00000344966.2:p.Pro19=
ENST00000529779.1:c.57C>G ENSP00000433912.1:p.Pro19=
NM_018105.2:c.57C>G NP_060575.1:p.Pro19=
NM_199003.1:c.57C>G NP_945354.1:p.Pro19=
NM_018105.3:c.57C>G MANE Select NP_060575.1:p.Pro19=
NM_199003.2:c.57C>G NP_945354.1:p.Pro19=