Canonical Allele Identifier: CA2366447937
Gene: PCIF1 HGNC NCBI

Linked Data

dbSNP Id: rs2083547982

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947782del , CM000682.2:g.45947782del GRCh38
NC_000020.10:g.44576421del , CM000682.1:g.44576421del GRCh37
NC_000020.9:g.44009828del NCBI36
NG_029772.1:g.29413del

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*27del MANE Select ENSP00000361486.3:n.*27del
ENST00000372409.7:c.*27del ENSP00000361486.3:n.*27del
ENST00000479348.2:c.1083del
NM_022104.3:c.*27del NP_071387.1:n.*27del
XM_011528980.1:c.*27del XP_011527282.1:n.*27del
XM_011528981.1:c.*27del XP_011527283.1:n.*27del
XM_011528982.1:c.*27del XP_011527284.1:n.*27del
XM_011528980.3:c.*27del XP_011527282.1:n.*27del
XM_011528981.3:c.*27del XP_011527283.1:n.*27del
XM_017028013.2:c.*27del XP_016883502.1:n.*27del
XM_017028014.2:c.*27del XP_016883503.1:n.*27del
NM_022104.4:c.*27del MANE Select NP_071387.1:n.*27del