Canonical Allele Identifier: CA371109437
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42698176G>C (hg19) chr8:g.42843033G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843033G>C , CM000670.2:g.42843033G>C GRCh38
NC_000008.10:g.42698176G>C , CM000670.1:g.42698176G>C GRCh37
NC_000008.9:g.42817333G>C NCBI36
NG_011837.1:g.5299C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.62C>G MANE Select ENSP00000254250.3:p.Ser21Cys
ENST00000345117.2:c.62C>G ENSP00000344966.2:p.Ser21Cys
ENST00000529779.1:c.62C>G ENSP00000433912.1:p.Ser21Cys
NM_018105.2:c.62C>G NP_060575.1:p.Ser21Cys
NM_199003.1:c.62C>G NP_945354.1:p.Ser21Cys
NM_018105.3:c.62C>G MANE Select NP_060575.1:p.Ser21Cys
NM_199003.2:c.62C>G NP_945354.1:p.Ser21Cys
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