Canonical Allele Identifier: CA2366447738
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947433_45947436delinsCAAG , CM000682.2:g.45947433_45947436delinsCAAG GRCh38
NC_000020.10:g.44576072_44576075delinsCAAG , CM000682.1:g.44576072_44576075delinsCAAG GRCh37
NC_000020.9:g.44009479_44009482delinsCAAG NCBI36
NG_029772.1:g.29759_29762delinsCTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1878_1881delinsCAAG MANE Select ENSP00000361486.3:p.Cys626=
ENST00000372409.7:c.1878_1881delinsCAAG ENSP00000361486.3:p.Cys626=
ENST00000479348.2:c.734_737delinsCAAG
NM_022104.3:c.1878_1881delinsCAAG NP_071387.1:p.Cys626=
XM_011528980.1:c.1878_1881delinsCAAG XP_011527282.1:p.Cys626=
XM_011528981.1:c.1878_1881delinsCAAG XP_011527283.1:p.Cys626=
XM_011528982.1:c.834_837delinsCAAG XP_011527284.1:p.Cys278=
XM_011528980.3:c.1878_1881delinsCAAG XP_011527282.1:p.Cys626=
XM_011528981.3:c.1878_1881delinsCAAG XP_011527283.1:p.Cys626=
XM_017028013.2:c.1878_1881delinsCAAG XP_016883502.1:p.Cys626=
XM_017028014.2:c.834_837delinsCAAG XP_016883503.1:p.Cys278=
NM_022104.4:c.1878_1881delinsCAAG MANE Select NP_071387.1:p.Cys626=