Canonical Allele Identifier: CA1779608021

Gene: THAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42838917_42838920delinsCTGA , CM000670.2:g.42838917_42838920delinsCTGA	GRCh38
NC_000008.10:g.42694060_42694063delinsCTGA , CM000670.1:g.42694060_42694063delinsCTGA	GRCh37
NC_000008.9:g.42813217_42813220delinsCTGA	NCBI36
NG_011837.1:g.9412_9415delinsTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.267+266_267+269delinsTCAG MANE Select	ENSP00000254250.3:n.267+266_267+269delinsTCAG
ENST00000345117.2:c.72-584_72-581delinsTCAG	ENSP00000344966.2:n.72-584_72-581delinsTCAG
ENST00000529779.1:c.267+266_267+269delinsTCAG	ENSP00000433912.1:n.267+266_267+269delinsTCAG
NM_018105.2:c.267+266_267+269delinsTCAG	NP_060575.1:n.267+266_267+269delinsTCAG
NM_199003.1:c.72-584_72-581delinsTCAG	NP_945354.1:n.72-584_72-581delinsTCAG
NM_018105.3:c.267+266_267+269delinsTCAG MANE Select	NP_060575.1:n.267+266_267+269delinsTCAG
NM_199003.2:c.72-584_72-581delinsTCAG	NP_945354.1:n.72-584_72-581delinsTCAG