Canonical Allele Identifier: CA2195380616
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966566C= , CM000677.2:g.90966566C= GRCh38
NC_000015.9:g.91509796C= , CM000677.1:g.91509796C= GRCh37
NC_000015.8:g.89310800C= NCBI36
NG_050647.1:g.33086G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*565G= (PRC1) MANE Select ENSP00000377793.3:n.*565G=
ENST00000643536.1:c.*4190G= ENSP00000494429.1:n.*4190G=
ENST00000361188.9:c.*565G= (PRC1) ENSP00000354679.5:n.*565G=
ENST00000394249.7:c.*565G= (PRC1) ENSP00000377793.3:n.*565G=
ENST00000555455.5:c.729G= (PRC1)
ENST00000556972.6:c.212G= (PRC1) ENSP00000456737.1:n.212G=
NM_001267580.1:c.*608G= (PRC1) NP_001254509.1:n.*608G=
NM_003981.3:c.*565G= (PRC1) NP_003972.1:n.*565G=
NM_199413.2:c.*565G= (PRC1) NP_955445.1:n.*565G=
NR_051984.1:n.198C= (PRC1-AS1)
XM_005254987.1:c.*608G= (PRC1) XP_005255044.1:n.*608G=
XM_006720759.1:c.*659G= (PRC1) XP_006720822.1:n.*659G=
XM_006720760.1:c.*71G= (PRC1) XP_006720823.1:n.*71G=
XM_011522187.1:c.*13G= (PRC1) XP_011520489.1:n.*13G=
XM_011522188.1:c.*13G= (PRC1) XP_011520490.1:n.*13G=
XM_011522189.1:c.*13G= (PRC1) XP_011520491.1:n.*13G=
XM_011522190.1:c.*13G= (PRC1) XP_011520492.1:n.*13G=
XM_011522192.1:c.*13G= (PRC1) XP_011520494.1:n.*13G=
XM_005254987.3:c.*608G= (PRC1) XP_005255044.1:n.*608G=
XM_006720759.2:c.*659G= (PRC1) XP_006720822.1:n.*659G=
XM_006720760.2:c.*71G= (PRC1) XP_006720823.1:n.*71G=
XM_011522187.2:c.*13G= (PRC1) XP_011520489.1:n.*13G=
XM_011522188.3:c.*13G= (PRC1) XP_011520490.1:n.*13G=
XM_011522189.2:c.*13G= (PRC1) XP_011520491.1:n.*13G=
XM_011522190.3:c.*13G= (PRC1) XP_011520492.1:n.*13G=
XM_011522191.3:c.*110G= (PRC1) XP_011520493.1:n.*110G=
XM_011522192.2:c.*13G= (PRC1) XP_011520494.1:n.*13G=
XM_017022712.2:c.*565G= (PRC1) XP_016878201.1:n.*565G=
XM_017022713.2:c.*565G= (PRC1) XP_016878202.1:n.*565G=
XM_017022714.2:c.*13G= (PRC1) XP_016878203.1:n.*13G=
XM_017022715.2:c.*565G= (PRC1) XP_016878204.1:n.*565G=
XM_017022716.2:c.*565G= (PRC1) XP_016878205.1:n.*565G=
XM_017022717.1:c.*608G= (PRC1) XP_016878206.1:n.*608G=
NM_003981.4:c.*565G= (PRC1) MANE Select NP_003972.2:n.*565G=
NM_001267580.2:c.*608G= (PRC1) NP_001254509.2:n.*608G=
NM_199413.3:c.*565G= (PRC1) NP_955445.2:n.*565G=