Canonical Allele Identifier: CA2687126236
Gene: THAP1 HGNC NCBI

Linked Data

gnomAD v4: 8-42839124-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839124A>C , CM000670.2:g.42839124A>C GRCh38
NC_000008.10:g.42694267A>C , CM000670.1:g.42694267A>C GRCh37
NC_000008.9:g.42813424A>C NCBI36
NG_011837.1:g.9208T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000254250.7:c.267+62T>G MANE Select ENSP00000254250.3:n.267+62T>G
ENST00000345117.2:c.72-788T>G ENSP00000344966.2:n.72-788T>G
ENST00000529779.1:c.267+62T>G ENSP00000433912.1:n.267+62T>G
NM_018105.2:c.267+62T>G NP_060575.1:n.267+62T>G
NM_199003.1:c.72-788T>G NP_945354.1:n.72-788T>G
NM_018105.3:c.267+62T>G MANE Select NP_060575.1:n.267+62T>G
NM_199003.2:c.72-788T>G NP_945354.1:n.72-788T>G
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