Canonical Allele Identifier: CA1779607922

Gene: THAP1

Linked Data

• dbSNP Id: rs1802662030

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42838739_42838742del , CM000670.2:g.42838739_42838742del	GRCh38
NC_000008.10:g.42693882_42693885del , CM000670.1:g.42693882_42693885del	GRCh37
NC_000008.9:g.42813039_42813042del	NCBI36
NG_011837.1:g.9593_9596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.268-403_268-400del MANE Select	ENSP00000254250.3:n.268-403_268-400del
ENST00000345117.2:c.72-403_72-400del	ENSP00000344966.2:n.72-403_72-400del
ENST00000529779.1:c.267+447_267+450del	ENSP00000433912.1:n.267+447_267+450del
NM_018105.2:c.268-403_268-400del	NP_060575.1:n.268-403_268-400del
NM_199003.1:c.72-403_72-400del	NP_945354.1:n.72-403_72-400del
NM_018105.3:c.268-403_268-400del MANE Select	NP_060575.1:n.268-403_268-400del
NM_199003.2:c.72-403_72-400del	NP_945354.1:n.72-403_72-400del