Canonical Allele Identifier: CA460569127

Gene: THAP1

Linked Data

• MyVariant Identifiers: chr8:g.42694437A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42839294A>T , CM000670.2:g.42839294A>T	GRCh38
NC_000008.10:g.42694437A>T , CM000670.1:g.42694437A>T	GRCh37
NC_000008.9:g.42813594A>T	NCBI36
NG_011837.1:g.9038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.159T>A MANE Select	ENSP00000254250.3:p.Ile53=
ENST00000345117.2:c.72-958T>A	ENSP00000344966.2:n.72-958T>A
ENST00000529779.1:c.159T>A	ENSP00000433912.1:p.Ile53=
ENST00000532093.1:n.389T>A
NM_018105.2:c.159T>A	NP_060575.1:p.Ile53=
NM_199003.1:c.72-958T>A	NP_945354.1:n.72-958T>A
NM_018105.3:c.159T>A MANE Select	NP_060575.1:p.Ile53=
NM_199003.2:c.72-958T>A	NP_945354.1:n.72-958T>A