Canonical Allele Identifier: CA2717208503
Gene: THAP1 HGNC NCBI

Linked Data

dbSNP Id: rs2128918548

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838755_42838763del , CM000670.2:g.42838755_42838763del GRCh38
NC_000008.10:g.42693898_42693906del , CM000670.1:g.42693898_42693906del GRCh37
NC_000008.9:g.42813055_42813063del NCBI36
NG_011837.1:g.9571_9579del

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.268-425_268-417del MANE Select ENSP00000254250.3:n.268-425_268-417del
ENST00000345117.2:c.72-425_72-417del ENSP00000344966.2:n.72-425_72-417del
ENST00000529779.1:c.267+425_267+433del ENSP00000433912.1:n.267+425_267+433del
NM_018105.2:c.268-425_268-417del NP_060575.1:n.268-425_268-417del
NM_199003.1:c.72-425_72-417del NP_945354.1:n.72-425_72-417del
NM_018105.3:c.268-425_268-417del MANE Select NP_060575.1:n.268-425_268-417del
NM_199003.2:c.72-425_72-417del NP_945354.1:n.72-425_72-417del