Canonical Allele Identifier: CA972730982
Gene: PRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1255036821

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966370_90966373del , CM000677.2:g.90966370_90966373del GRCh38
NC_000015.9:g.91509600_91509603del , CM000677.1:g.91509600_91509603del GRCh37
NC_000015.8:g.89310604_89310607del NCBI36
NG_050647.1:g.33283_33286del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*762_*765del MANE Select ENSP00000377793.3:n.*762_*765del
ENST00000643536.1:c.*4387_*4390del ENSP00000494429.1:n.*4387_*4390del
ENST00000361188.9:c.*762_*765del ENSP00000354679.5:n.*762_*765del
ENST00000394249.7:c.*762_*765del ENSP00000377793.3:n.*762_*765del
ENST00000556972.6:c.409_412del ENSP00000456737.1:n.409_412del
NM_001267580.1:c.*805_*808del NP_001254509.1:n.*805_*808del
NM_003981.3:c.*762_*765del NP_003972.1:n.*762_*765del
NM_199413.2:c.*762_*765del NP_955445.1:n.*762_*765del
XM_005254987.1:c.*805_*808del XP_005255044.1:n.*805_*808del
XM_006720759.1:c.*856_*859del XP_006720822.1:n.*856_*859del
XM_006720760.1:c.*268_*271del XP_006720823.1:n.*268_*271del
XM_011522187.1:c.*210_*213del XP_011520489.1:n.*210_*213del
XM_011522188.1:c.*210_*213del XP_011520490.1:n.*210_*213del
XM_011522189.1:c.*210_*213del XP_011520491.1:n.*210_*213del
XM_011522190.1:c.*210_*213del XP_011520492.1:n.*210_*213del
XM_011522192.1:c.*210_*213del XP_011520494.1:n.*210_*213del
XM_005254987.3:c.*805_*808del XP_005255044.1:n.*805_*808del
XM_006720759.2:c.*856_*859del XP_006720822.1:n.*856_*859del
XM_006720760.2:c.*268_*271del XP_006720823.1:n.*268_*271del
XM_011522187.2:c.*210_*213del XP_011520489.1:n.*210_*213del
XM_011522188.3:c.*210_*213del XP_011520490.1:n.*210_*213del
XM_011522189.2:c.*210_*213del XP_011520491.1:n.*210_*213del
XM_011522191.3:c.*307_*310del XP_011520493.1:n.*307_*310del
XM_011522192.2:c.*210_*213del XP_011520494.1:n.*210_*213del
XM_017022712.2:c.*762_*765del XP_016878201.1:n.*762_*765del
XM_017022713.2:c.*762_*765del XP_016878202.1:n.*762_*765del
XM_017022715.2:c.*762_*765del XP_016878204.1:n.*762_*765del
XM_017022716.2:c.*762_*765del XP_016878205.1:n.*762_*765del
XM_017022717.1:c.*805_*808del XP_016878206.1:n.*805_*808del
NM_003981.4:c.*762_*765del MANE Select NP_003972.2:n.*762_*765del
NM_001267580.2:c.*805_*808del NP_001254509.2:n.*805_*808del
NM_199413.3:c.*762_*765del NP_955445.2:n.*762_*765del