Canonical Allele Identifier: CA371109441
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42698177A>T (hg19) chr8:g.42843034A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843034A>T , CM000670.2:g.42843034A>T GRCh38
NC_000008.10:g.42698177A>T , CM000670.1:g.42698177A>T GRCh37
NC_000008.9:g.42817334A>T NCBI36
NG_011837.1:g.5298T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.61T>A MANE Select ENSP00000254250.3:p.Ser21Thr
ENST00000345117.2:c.61T>A ENSP00000344966.2:p.Ser21Thr
ENST00000529779.1:c.61T>A ENSP00000433912.1:p.Ser21Thr
NM_018105.2:c.61T>A NP_060575.1:p.Ser21Thr
NM_199003.1:c.61T>A NP_945354.1:p.Ser21Thr
NM_018105.3:c.61T>A MANE Select NP_060575.1:p.Ser21Thr
NM_199003.2:c.61T>A NP_945354.1:p.Ser21Thr
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