Canonical Allele Identifier: CA2366447988
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947863T= , CM000682.2:g.45947863T= GRCh38
NC_000020.10:g.44576502T= , CM000682.1:g.44576502T= GRCh37
NC_000020.9:g.44009909T= NCBI36
NG_029772.1:g.29332A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*108T= MANE Select ENSP00000361486.3:n.*108T=
ENST00000372409.7:c.*108T= ENSP00000361486.3:n.*108T=
ENST00000479348.2:c.1164T=
NM_022104.3:c.*108T= NP_071387.1:n.*108T=
XM_011528980.1:c.*108T= XP_011527282.1:n.*108T=
XM_011528981.1:c.*108T= XP_011527283.1:n.*108T=
XM_011528982.1:c.*108T= XP_011527284.1:n.*108T=
XM_011528980.3:c.*108T= XP_011527282.1:n.*108T=
XM_011528981.3:c.*108T= XP_011527283.1:n.*108T=
XM_017028013.2:c.*108T= XP_016883502.1:n.*108T=
XM_017028014.2:c.*108T= XP_016883503.1:n.*108T=
NM_022104.4:c.*108T= MANE Select NP_071387.1:n.*108T=