Canonical Allele Identifier: CA2653107650
Gene: PCIF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45947795_45947796del , CM000682.2:g.45947795_45947796del GRCh38
NC_000020.10:g.44576434_44576435del , CM000682.1:g.44576434_44576435del GRCh37
NC_000020.9:g.44009841_44009842del NCBI36
NG_029772.1:g.29399_29400del

Transcript Alleles

HGVS Amino-acid change
ENST00000372409.8:c.*40_*41del MANE Select ENSP00000361486.3:n.*40_*41del
ENST00000372409.7:c.*40_*41del ENSP00000361486.3:n.*40_*41del
ENST00000479348.2:c.1096_1097del
NM_022104.3:c.*40_*41del NP_071387.1:n.*40_*41del
XM_011528980.1:c.*40_*41del XP_011527282.1:n.*40_*41del
XM_011528981.1:c.*40_*41del XP_011527283.1:n.*40_*41del
XM_011528982.1:c.*40_*41del XP_011527284.1:n.*40_*41del
XM_011528980.3:c.*40_*41del XP_011527282.1:n.*40_*41del
XM_011528981.3:c.*40_*41del XP_011527283.1:n.*40_*41del
XM_017028013.2:c.*40_*41del XP_016883502.1:n.*40_*41del
XM_017028014.2:c.*40_*41del XP_016883503.1:n.*40_*41del
NM_022104.4:c.*40_*41del MANE Select NP_071387.1:n.*40_*41del