Canonical Allele Identifier: CA2653107571
Gene: PCIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947736del , CM000682.2:g.45947736del GRCh38
NC_000020.10:g.44576375del , CM000682.1:g.44576375del GRCh37
NC_000020.9:g.44009782del NCBI36
NG_029772.1:g.29459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.2096del MANE Select ENSP00000361486.3:p.Arg699ProfsTer19
ENST00000372409.7:c.2096del ENSP00000361486.3:p.Arg699ProfsTer19
ENST00000479348.2:c.1037del
NM_022104.3:c.2096del NP_071387.1:p.Arg699ProfsTer19
XM_011528980.1:c.2096del XP_011527282.1:p.Arg699ProfsTer19
XM_011528981.1:c.2096del XP_011527283.1:p.Arg699ProfsTer19
XM_011528982.1:c.1052del XP_011527284.1:p.Arg351ProfsTer19
XM_011528980.3:c.2096del XP_011527282.1:p.Arg699ProfsTer19
XM_011528981.3:c.2096del XP_011527283.1:p.Arg699ProfsTer19
XM_017028013.2:c.2096del XP_016883502.1:p.Arg699ProfsTer19
XM_017028014.2:c.1052del XP_016883503.1:p.Arg351ProfsTer19
NM_022104.4:c.2096del MANE Select NP_071387.1:p.Arg699ProfsTer19