Canonical Allele Identifier: CA2366447919
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947767_45947770delinsGGGA , CM000682.2:g.45947767_45947770delinsGGGA GRCh38
NC_000020.10:g.44576406_44576409delinsGGGA , CM000682.1:g.44576406_44576409delinsGGGA GRCh37
NC_000020.9:g.44009813_44009816delinsGGGA NCBI36
NG_029772.1:g.29425_29428delinsTCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*12_*15delinsGGGA MANE Select ENSP00000361486.3:n.*12_*15delinsGGGA
ENST00000372409.7:c.*12_*15delinsGGGA ENSP00000361486.3:n.*12_*15delinsGGGA
ENST00000479348.2:c.1068_1071delinsGGGA
NM_022104.3:c.*12_*15delinsGGGA NP_071387.1:n.*12_*15delinsGGGA
XM_011528980.1:c.*12_*15delinsGGGA XP_011527282.1:n.*12_*15delinsGGGA
XM_011528981.1:c.*12_*15delinsGGGA XP_011527283.1:n.*12_*15delinsGGGA
XM_011528982.1:c.*12_*15delinsGGGA XP_011527284.1:n.*12_*15delinsGGGA
XM_011528980.3:c.*12_*15delinsGGGA XP_011527282.1:n.*12_*15delinsGGGA
XM_011528981.3:c.*12_*15delinsGGGA XP_011527283.1:n.*12_*15delinsGGGA
XM_017028013.2:c.*12_*15delinsGGGA XP_016883502.1:n.*12_*15delinsGGGA
XM_017028014.2:c.*12_*15delinsGGGA XP_016883503.1:n.*12_*15delinsGGGA
NM_022104.4:c.*12_*15delinsGGGA MANE Select NP_071387.1:n.*12_*15delinsGGGA