Canonical Allele Identifier: CA1779607923

Gene: THAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42838741_42838742delinsCT , CM000670.2:g.42838741_42838742delinsCT	GRCh38
NC_000008.10:g.42693884_42693885delinsCT , CM000670.1:g.42693884_42693885delinsCT	GRCh37
NC_000008.9:g.42813041_42813042delinsCT	NCBI36
NG_011837.1:g.9590_9591delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.268-406_268-405delinsAG MANE Select	ENSP00000254250.3:n.268-406_268-405delinsAG
ENST00000345117.2:c.72-406_72-405delinsAG	ENSP00000344966.2:n.72-406_72-405delinsAG
ENST00000529779.1:c.267+444_267+445delinsAG	ENSP00000433912.1:n.267+444_267+445delinsAG
NM_018105.2:c.268-406_268-405delinsAG	NP_060575.1:n.268-406_268-405delinsAG
NM_199003.1:c.72-406_72-405delinsAG	NP_945354.1:n.72-406_72-405delinsAG
NM_018105.3:c.268-406_268-405delinsAG MANE Select	NP_060575.1:n.268-406_268-405delinsAG
NM_199003.2:c.72-406_72-405delinsAG	NP_945354.1:n.72-406_72-405delinsAG