Canonical Allele Identifier: CA2577413325
Gene: PCIF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947482_45947487del , CM000682.2:g.45947482_45947487del GRCh38
NC_000020.10:g.44576121_44576126del , CM000682.1:g.44576121_44576126del GRCh37
NC_000020.9:g.44009528_44009533del NCBI36
NG_029772.1:g.29709_29714del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372409.8:c.1884-42_1884-37del MANE Select ENSP00000361486.3:n.1884-42_1884-37del
ENST00000372409.7:c.1884-42_1884-37del ENSP00000361486.3:n.1884-42_1884-37del
ENST00000479348.2:c.783_788del
NM_022104.3:c.1884-42_1884-37del NP_071387.1:n.1884-42_1884-37del
XM_011528980.1:c.1884-42_1884-37del XP_011527282.1:n.1884-42_1884-37del
XM_011528981.1:c.1884-42_1884-37del XP_011527283.1:n.1884-42_1884-37del
XM_011528982.1:c.840-42_840-37del XP_011527284.1:n.840-42_840-37del
XM_011528980.3:c.1884-42_1884-37del XP_011527282.1:n.1884-42_1884-37del
XM_011528981.3:c.1884-42_1884-37del XP_011527283.1:n.1884-42_1884-37del
XM_017028013.2:c.1884-42_1884-37del XP_016883502.1:n.1884-42_1884-37del
XM_017028014.2:c.840-42_840-37del XP_016883503.1:n.840-42_840-37del
NM_022104.4:c.1884-42_1884-37del MANE Select NP_071387.1:n.1884-42_1884-37del