Canonical Allele Identifier: CA2366447729
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947415T= , CM000682.2:g.45947415T= GRCh38
NC_000020.10:g.44576054T= , CM000682.1:g.44576054T= GRCh37
NC_000020.9:g.44009461T= NCBI36
NG_029772.1:g.29780A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1860T= MANE Select ENSP00000361486.3:p.Ser620=
ENST00000372409.7:c.1860T= ENSP00000361486.3:p.Ser620=
ENST00000479348.2:c.716T=
NM_022104.3:c.1860T= NP_071387.1:p.Ser620=
XM_011528980.1:c.1860T= XP_011527282.1:p.Ser620=
XM_011528981.1:c.1860T= XP_011527283.1:p.Ser620=
XM_011528982.1:c.816T= XP_011527284.1:p.Ser272=
XM_011528980.3:c.1860T= XP_011527282.1:p.Ser620=
XM_011528981.3:c.1860T= XP_011527283.1:p.Ser620=
XM_017028013.2:c.1860T= XP_016883502.1:p.Ser620=
XM_017028014.2:c.816T= XP_016883503.1:p.Ser272=
NM_022104.4:c.1860T= MANE Select NP_071387.1:p.Ser620=