Canonical Allele Identifier: CA2366447939
Gene: PCIF1 HGNC NCBI

Linked Data

dbSNP Id: rs2083548007

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947786del , CM000682.2:g.45947786del GRCh38
NC_000020.10:g.44576425del , CM000682.1:g.44576425del GRCh37
NC_000020.9:g.44009832del NCBI36
NG_029772.1:g.29412del

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*31del MANE Select ENSP00000361486.3:n.*31del
ENST00000372409.7:c.*31del ENSP00000361486.3:n.*31del
ENST00000479348.2:c.1087del
NM_022104.3:c.*31del NP_071387.1:n.*31del
XM_011528980.1:c.*31del XP_011527282.1:n.*31del
XM_011528981.1:c.*31del XP_011527283.1:n.*31del
XM_011528982.1:c.*31del XP_011527284.1:n.*31del
XM_011528980.3:c.*31del XP_011527282.1:n.*31del
XM_011528981.3:c.*31del XP_011527283.1:n.*31del
XM_017028013.2:c.*31del XP_016883502.1:n.*31del
XM_017028014.2:c.*31del XP_016883503.1:n.*31del
NM_022104.4:c.*31del MANE Select NP_071387.1:n.*31del