Canonical Allele Identifier: CA2974733722
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947768_45947769del , CM000682.2:g.45947768_45947769del GRCh38
NC_000020.10:g.44576407_44576408del , CM000682.1:g.44576407_44576408del GRCh37
NC_000020.9:g.44009814_44009815del NCBI36
NG_029772.1:g.29428_29429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.*13_*14del MANE Select ENSP00000361486.3:n.*13_*14del
ENST00000372409.7:c.*13_*14del ENSP00000361486.3:n.*13_*14del
ENST00000479348.2:c.1069_1070del
NM_022104.3:c.*13_*14del NP_071387.1:n.*13_*14del
XM_011528980.1:c.*13_*14del XP_011527282.1:n.*13_*14del
XM_011528981.1:c.*13_*14del XP_011527283.1:n.*13_*14del
XM_011528982.1:c.*13_*14del XP_011527284.1:n.*13_*14del
XM_011528980.3:c.*13_*14del XP_011527282.1:n.*13_*14del
XM_011528981.3:c.*13_*14del XP_011527283.1:n.*13_*14del
XM_017028013.2:c.*13_*14del XP_016883502.1:n.*13_*14del
XM_017028014.2:c.*13_*14del XP_016883503.1:n.*13_*14del
NM_022104.4:c.*13_*14del MANE Select NP_071387.1:n.*13_*14del