Canonical Allele Identifier: CA371109452
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42698183G>T (hg19) chr8:g.42843040G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843040G>T , CM000670.2:g.42843040G>T GRCh38
NC_000008.10:g.42698183G>T , CM000670.1:g.42698183G>T GRCh37
NC_000008.9:g.42817340G>T NCBI36
NG_011837.1:g.5292C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.55C>A MANE Select ENSP00000254250.3:p.Pro19Thr
ENST00000345117.2:c.55C>A ENSP00000344966.2:p.Pro19Thr
ENST00000529779.1:c.55C>A ENSP00000433912.1:p.Pro19Thr
NM_018105.2:c.55C>A NP_060575.1:p.Pro19Thr
NM_199003.1:c.55C>A NP_945354.1:p.Pro19Thr
NM_018105.3:c.55C>A MANE Select NP_060575.1:p.Pro19Thr
NM_199003.2:c.55C>A NP_945354.1:p.Pro19Thr
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