Canonical Allele Identifier: CA2195380677
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966598G= , CM000677.2:g.90966598G= GRCh38
NC_000015.9:g.91509828G= , CM000677.1:g.91509828G= GRCh37
NC_000015.8:g.89310832G= NCBI36
NG_050647.1:g.33054C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*533C= (PRC1) MANE Select ENSP00000377793.3:n.*533C=
ENST00000643536.1:c.*4158C= ENSP00000494429.1:n.*4158C=
ENST00000361188.9:c.*533C= (PRC1) ENSP00000354679.5:n.*533C=
ENST00000394249.7:c.*533C= (PRC1) ENSP00000377793.3:n.*533C=
ENST00000555455.5:c.697C= (PRC1)
ENST00000556972.6:c.180C= (PRC1) ENSP00000456737.1:n.180C=
NM_001267580.1:c.*576C= (PRC1) NP_001254509.1:n.*576C=
NM_003981.3:c.*533C= (PRC1) NP_003972.1:n.*533C=
NM_199413.2:c.*533C= (PRC1) NP_955445.1:n.*533C=
NR_051984.1:n.230G= (PRC1-AS1)
XM_005254987.1:c.*576C= (PRC1) XP_005255044.1:n.*576C=
XM_006720759.1:c.*627C= (PRC1) XP_006720822.1:n.*627C=
XM_006720760.1:c.*39C= (PRC1) XP_006720823.1:n.*39C=
XM_011522187.1:c.1847C= (PRC1) XP_011520489.1:p.Ala616=
XM_011522188.1:c.1805C= (PRC1) XP_011520490.1:p.Ala602=
XM_011522189.1:c.1736C= (PRC1) XP_011520491.1:p.Ala579=
XM_011522190.1:c.1676C= (PRC1) XP_011520492.1:p.Ala559=
XM_011522191.1:c.*78C= (PRC1) XP_011520493.1:n.*78C=
XM_011522192.1:c.1526C= (PRC1) XP_011520494.1:p.Ala509=
XM_005254987.3:c.*576C= (PRC1) XP_005255044.1:n.*576C=
XM_006720759.2:c.*627C= (PRC1) XP_006720822.1:n.*627C=
XM_006720760.2:c.*39C= (PRC1) XP_006720823.1:n.*39C=
XM_011522187.2:c.1847C= (PRC1) XP_011520489.1:p.Ala616=
XM_011522188.3:c.1805C= (PRC1) XP_011520490.1:p.Ala602=
XM_011522189.2:c.1736C= (PRC1) XP_011520491.1:p.Ala579=
XM_011522190.3:c.1676C= (PRC1) XP_011520492.1:p.Ala559=
XM_011522191.3:c.*78C= (PRC1) XP_011520493.1:n.*78C=
XM_011522192.2:c.1526C= (PRC1) XP_011520494.1:p.Ala509=
XM_017022712.2:c.*533C= (PRC1) XP_016878201.1:n.*533C=
XM_017022713.2:c.*533C= (PRC1) XP_016878202.1:n.*533C=
XM_017022714.2:c.1691C= (PRC1) XP_016878203.1:p.Ala564=
XM_017022715.2:c.*533C= (PRC1) XP_016878204.1:n.*533C=
XM_017022716.2:c.*533C= (PRC1) XP_016878205.1:n.*533C=
XM_017022717.1:c.*576C= (PRC1) XP_016878206.1:n.*576C=
NM_003981.4:c.*533C= (PRC1) MANE Select NP_003972.2:n.*533C=
NM_001267580.2:c.*576C= (PRC1) NP_001254509.2:n.*576C=
NM_199413.3:c.*533C= (PRC1) NP_955445.2:n.*533C=