Canonical Allele Identifier: CA371107798
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42694395G>T (hg19) chr8:g.42839252G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839252G>T , CM000670.2:g.42839252G>T GRCh38
NC_000008.10:g.42694395G>T , CM000670.1:g.42694395G>T GRCh37
NC_000008.9:g.42813552G>T NCBI36
NG_011837.1:g.9080C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.201C>A MANE Select ENSP00000254250.3:p.Cys67Ter
ENST00000345117.2:c.72-916C>A ENSP00000344966.2:n.72-916C>A
ENST00000529779.1:c.201C>A ENSP00000433912.1:p.Cys67Ter
ENST00000532093.1:n.431C>A
NM_018105.2:c.201C>A NP_060575.1:p.Cys67Ter
NM_199003.1:c.72-916C>A NP_945354.1:n.72-916C>A
NM_018105.3:c.201C>A MANE Select NP_060575.1:p.Cys67Ter
NM_199003.2:c.72-916C>A NP_945354.1:n.72-916C>A
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