Canonical Allele Identifier: CA2630413971
Gene: PRC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966253_90966266dup , CM000677.2:g.90966253_90966266dup GRCh38
NC_000015.9:g.91509483_91509496dup , CM000677.1:g.91509483_91509496dup GRCh37
NC_000015.8:g.89310487_89310500dup NCBI36
NG_050647.1:g.33386_33399dup

Transcript Alleles

HGVS Amino-acid change
ENST00000394249.8:c.*865_*878dup MANE Select ENSP00000377793.3:n.*865_*878dup
ENST00000643536.1:c.*4490_*4503dup ENSP00000494429.1:n.*4490_*4503dup
ENST00000361188.9:c.*865_*878dup ENSP00000354679.5:n.*865_*878dup
ENST00000394249.7:c.*865_*878dup ENSP00000377793.3:n.*865_*878dup
ENST00000556972.6:c.512_525dup ENSP00000456737.1:n.512_525dup
NM_001267580.1:c.*908_*921dup NP_001254509.1:n.*908_*921dup
NM_003981.3:c.*865_*878dup NP_003972.1:n.*865_*878dup
NM_199413.2:c.*865_*878dup NP_955445.1:n.*865_*878dup
XM_005254987.1:c.*908_*921dup XP_005255044.1:n.*908_*921dup
XM_006720759.1:c.*959_*972dup XP_006720822.1:n.*959_*972dup
XM_006720760.1:c.*371_*384dup XP_006720823.1:n.*371_*384dup
XM_011522187.1:c.*313_*326dup XP_011520489.1:n.*313_*326dup
XM_011522188.1:c.*313_*326dup XP_011520490.1:n.*313_*326dup
XM_011522189.1:c.*313_*326dup XP_011520491.1:n.*313_*326dup
XM_011522190.1:c.*313_*326dup XP_011520492.1:n.*313_*326dup
XM_011522192.1:c.*313_*326dup XP_011520494.1:n.*313_*326dup
XM_005254987.3:c.*908_*921dup XP_005255044.1:n.*908_*921dup
XM_006720759.2:c.*959_*972dup XP_006720822.1:n.*959_*972dup
XM_006720760.2:c.*371_*384dup XP_006720823.1:n.*371_*384dup
XM_011522187.2:c.*313_*326dup XP_011520489.1:n.*313_*326dup
XM_011522188.3:c.*313_*326dup XP_011520490.1:n.*313_*326dup
XM_011522189.2:c.*313_*326dup XP_011520491.1:n.*313_*326dup
XM_011522191.3:c.*410_*423dup XP_011520493.1:n.*410_*423dup
XM_011522192.2:c.*313_*326dup XP_011520494.1:n.*313_*326dup
XM_017022712.2:c.*865_*878dup XP_016878201.1:n.*865_*878dup
XM_017022713.2:c.*865_*878dup XP_016878202.1:n.*865_*878dup
XM_017022715.2:c.*865_*878dup XP_016878204.1:n.*865_*878dup
XM_017022716.2:c.*865_*878dup XP_016878205.1:n.*865_*878dup
XM_017022717.1:c.*908_*921dup XP_016878206.1:n.*908_*921dup
NM_003981.4:c.*865_*878dup MANE Select NP_003972.2:n.*865_*878dup
NM_001267580.2:c.*908_*921dup NP_001254509.2:n.*908_*921dup
NM_199413.3:c.*865_*878dup NP_955445.2:n.*865_*878dup