Canonical Allele Identifier: CA717052883
Gene: PRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1163619954

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966188del , CM000677.2:g.90966188del GRCh38
NC_000015.9:g.91509418del , CM000677.1:g.91509418del GRCh37
NC_000015.8:g.89310422del NCBI36
NG_050647.1:g.33464del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*943del MANE Select ENSP00000377793.3:n.*943del
ENST00000361188.9:c.*943del ENSP00000354679.5:n.*943del
ENST00000394249.7:c.*943del ENSP00000377793.3:n.*943del
ENST00000556972.6:c.590del ENSP00000456737.1:n.590del
NM_001267580.1:c.*986del NP_001254509.1:n.*986del
NM_003981.3:c.*943del NP_003972.1:n.*943del
NM_199413.2:c.*943del NP_955445.1:n.*943del
XM_005254987.1:c.*986del XP_005255044.1:n.*986del
XM_006720759.1:c.*1037del XP_006720822.1:n.*1037del
XM_006720760.1:c.*449del XP_006720823.1:n.*449del
XM_011522187.1:c.*391del XP_011520489.1:n.*391del
XM_011522188.1:c.*391del XP_011520490.1:n.*391del
XM_011522189.1:c.*391del XP_011520491.1:n.*391del
XM_011522190.1:c.*391del XP_011520492.1:n.*391del
XM_011522192.1:c.*391del XP_011520494.1:n.*391del
XM_005254987.3:c.*986del XP_005255044.1:n.*986del
XM_006720759.2:c.*1037del XP_006720822.1:n.*1037del
XM_006720760.2:c.*449del XP_006720823.1:n.*449del
XM_011522187.2:c.*391del XP_011520489.1:n.*391del
XM_011522188.3:c.*391del XP_011520490.1:n.*391del
XM_011522189.2:c.*391del XP_011520491.1:n.*391del
XM_011522191.3:c.*488del XP_011520493.1:n.*488del
XM_011522192.2:c.*391del XP_011520494.1:n.*391del
XM_017022712.2:c.*943del XP_016878201.1:n.*943del
XM_017022713.2:c.*943del XP_016878202.1:n.*943del
XM_017022715.2:c.*943del XP_016878204.1:n.*943del
XM_017022716.2:c.*943del XP_016878205.1:n.*943del
XM_017022717.1:c.*986del XP_016878206.1:n.*986del
NM_003981.4:c.*943del MANE Select NP_003972.2:n.*943del
NM_001267580.2:c.*986del NP_001254509.2:n.*986del
NM_199413.3:c.*943del NP_955445.2:n.*943del