Canonical Allele Identifier: CA2366447818
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947590T= , CM000682.2:g.45947590T= GRCh38
NC_000020.10:g.44576229T= , CM000682.1:g.44576229T= GRCh37
NC_000020.9:g.44009636T= NCBI36
NG_029772.1:g.29605A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1950T= MANE Select ENSP00000361486.3:p.Phe650=
ENST00000372409.7:c.1950T= ENSP00000361486.3:p.Phe650=
ENST00000479348.2:c.891T=
NM_022104.3:c.1950T= NP_071387.1:p.Phe650=
XM_011528980.1:c.1950T= XP_011527282.1:p.Phe650=
XM_011528981.1:c.1950T= XP_011527283.1:p.Phe650=
XM_011528982.1:c.906T= XP_011527284.1:p.Phe302=
XM_011528980.3:c.1950T= XP_011527282.1:p.Phe650=
XM_011528981.3:c.1950T= XP_011527283.1:p.Phe650=
XM_017028013.2:c.1950T= XP_016883502.1:p.Phe650=
XM_017028014.2:c.906T= XP_016883503.1:p.Phe302=
NM_022104.4:c.1950T= MANE Select NP_071387.1:p.Phe650=