Canonical Allele Identifier: CA371107796

Gene: THAP1

Linked Data

• MyVariant Identifiers: chr8:g.42694394T>A (hg19) ; chr8:g.42839251T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42839251T>A , CM000670.2:g.42839251T>A	GRCh38
NC_000008.10:g.42694394T>A , CM000670.1:g.42694394T>A	GRCh37
NC_000008.9:g.42813551T>A	NCBI36
NG_011837.1:g.9081A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.202A>T MANE Select	ENSP00000254250.3:p.Asn68Tyr
ENST00000345117.2:c.72-915A>T	ENSP00000344966.2:n.72-915A>T
ENST00000529779.1:c.202A>T	ENSP00000433912.1:p.Asn68Tyr
ENST00000532093.1:n.432A>T
NM_018105.2:c.202A>T	NP_060575.1:p.Asn68Tyr
NM_199003.1:c.72-915A>T	NP_945354.1:n.72-915A>T
NM_018105.3:c.202A>T MANE Select	NP_060575.1:p.Asn68Tyr
NM_199003.2:c.72-915A>T	NP_945354.1:n.72-915A>T