Canonical Allele Identifier: CA492187248
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1420537008

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966409G>C , CM000677.2:g.90966409G>C GRCh38
NC_000015.9:g.91509639G>C , CM000677.1:g.91509639G>C GRCh37
NC_000015.8:g.89310643G>C NCBI36
NG_050647.1:g.33243C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*722C>G (PRC1) MANE Select ENSP00000377793.3:n.*722C>G
ENST00000643536.1:c.*4347C>G ENSP00000494429.1:n.*4347C>G
ENST00000361188.9:c.*722C>G (PRC1) ENSP00000354679.5:n.*722C>G
ENST00000394249.7:c.*722C>G (PRC1) ENSP00000377793.3:n.*722C>G
ENST00000556972.6:c.369C>G (PRC1) ENSP00000456737.1:n.369C>G
NM_001267580.1:c.*765C>G (PRC1) NP_001254509.1:n.*765C>G
NM_003981.3:c.*722C>G (PRC1) NP_003972.1:n.*722C>G
NM_199413.2:c.*722C>G (PRC1) NP_955445.1:n.*722C>G
NR_051984.1:n.41G>C (PRC1-AS1)
XM_005254987.1:c.*765C>G (PRC1) XP_005255044.1:n.*765C>G
XM_006720759.1:c.*816C>G (PRC1) XP_006720822.1:n.*816C>G
XM_006720760.1:c.*228C>G (PRC1) XP_006720823.1:n.*228C>G
XM_011522187.1:c.*170C>G (PRC1) XP_011520489.1:n.*170C>G
XM_011522188.1:c.*170C>G (PRC1) XP_011520490.1:n.*170C>G
XM_011522189.1:c.*170C>G (PRC1) XP_011520491.1:n.*170C>G
XM_011522190.1:c.*170C>G (PRC1) XP_011520492.1:n.*170C>G
XM_011522192.1:c.*170C>G (PRC1) XP_011520494.1:n.*170C>G
XM_005254987.3:c.*765C>G (PRC1) XP_005255044.1:n.*765C>G
XM_006720759.2:c.*816C>G (PRC1) XP_006720822.1:n.*816C>G
XM_006720760.2:c.*228C>G (PRC1) XP_006720823.1:n.*228C>G
XM_011522187.2:c.*170C>G (PRC1) XP_011520489.1:n.*170C>G
XM_011522188.3:c.*170C>G (PRC1) XP_011520490.1:n.*170C>G
XM_011522189.2:c.*170C>G (PRC1) XP_011520491.1:n.*170C>G
XM_011522191.3:c.*267C>G (PRC1) XP_011520493.1:n.*267C>G
XM_011522192.2:c.*170C>G (PRC1) XP_011520494.1:n.*170C>G
XM_017022712.2:c.*722C>G (PRC1) XP_016878201.1:n.*722C>G
XM_017022713.2:c.*722C>G (PRC1) XP_016878202.1:n.*722C>G
XM_017022715.2:c.*722C>G (PRC1) XP_016878204.1:n.*722C>G
XM_017022716.2:c.*722C>G (PRC1) XP_016878205.1:n.*722C>G
XM_017022717.1:c.*765C>G (PRC1) XP_016878206.1:n.*765C>G
NM_003981.4:c.*722C>G (PRC1) MANE Select NP_003972.2:n.*722C>G
NM_001267580.2:c.*765C>G (PRC1) NP_001254509.2:n.*765C>G
NM_199413.3:c.*722C>G (PRC1) NP_955445.2:n.*722C>G