Canonical Allele Identifier: CA2366447884
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947708G= , CM000682.2:g.45947708G= GRCh38
NC_000020.10:g.44576347G= , CM000682.1:g.44576347G= GRCh37
NC_000020.9:g.44009754G= NCBI36
NG_029772.1:g.29487C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.2068G= MANE Select ENSP00000361486.3:p.Asp690=
ENST00000372409.7:c.2068G= ENSP00000361486.3:p.Asp690=
ENST00000479348.2:c.1009G=
NM_022104.3:c.2068G= NP_071387.1:p.Asp690=
XM_011528980.1:c.2068G= XP_011527282.1:p.Asp690=
XM_011528981.1:c.2068G= XP_011527283.1:p.Asp690=
XM_011528982.1:c.1024G= XP_011527284.1:p.Asp342=
XM_011528980.3:c.2068G= XP_011527282.1:p.Asp690=
XM_011528981.3:c.2068G= XP_011527283.1:p.Asp690=
XM_017028013.2:c.2068G= XP_016883502.1:p.Asp690=
XM_017028014.2:c.1024G= XP_016883503.1:p.Asp342=
NM_022104.4:c.2068G= MANE Select NP_071387.1:p.Asp690=