Canonical Allele Identifier: CA717053272
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1281628260

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966748_90966751dup , CM000677.2:g.90966748_90966751dup GRCh38
NC_000015.9:g.91509978_91509981dup , CM000677.1:g.91509978_91509981dup GRCh37
NC_000015.8:g.89310982_89310985dup NCBI36
NG_050647.1:g.32903_32906dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*382_*385dup (PRC1) MANE Select ENSP00000377793.3:n.*382_*385dup
ENST00000643536.1:c.*4007_*4010dup ENSP00000494429.1:n.*4007_*4010dup
ENST00000361188.9:c.*382_*385dup (PRC1) ENSP00000354679.5:n.*382_*385dup
ENST00000394249.7:c.*382_*385dup (PRC1) ENSP00000377793.3:n.*382_*385dup
ENST00000555455.5:c.642-96_642-93dup (PRC1)
ENST00000556972.6:c.125-96_125-93dup (PRC1) ENSP00000456737.1:n.125-96_125-93dup
ENST00000560423.5:c.670_673dup (PRC1)
NM_001267580.1:c.*425_*428dup (PRC1) NP_001254509.1:n.*425_*428dup
NM_003981.3:c.*382_*385dup (PRC1) NP_003972.1:n.*382_*385dup
NM_199413.2:c.*382_*385dup (PRC1) NP_955445.1:n.*382_*385dup
NR_051984.1:n.310+70_310+73dup (PRC1-AS1)
XM_005254987.1:c.*425_*428dup (PRC1) XP_005255044.1:n.*425_*428dup
XM_006720759.1:c.*476_*479dup (PRC1) XP_006720822.1:n.*476_*479dup
XM_006720760.1:c.1673-96_1673-93dup (PRC1) XP_006720823.1:n.1673-96_1673-93dup
XM_011522187.1:c.1792-96_1792-93dup (PRC1) XP_011520489.1:n.1792-96_1792-93dup
XM_011522188.1:c.1750-96_1750-93dup (PRC1) XP_011520490.1:n.1750-96_1750-93dup
XM_011522189.1:c.1681-96_1681-93dup (PRC1) XP_011520491.1:n.1681-96_1681-93dup
XM_011522190.1:c.1621-96_1621-93dup (PRC1) XP_011520492.1:n.1621-96_1621-93dup
XM_011522191.1:c.*23-96_*23-93dup (PRC1) XP_011520493.1:n.*23-96_*23-93dup
XM_011522192.1:c.1471-96_1471-93dup (PRC1) XP_011520494.1:n.1471-96_1471-93dup
XM_005254987.3:c.*425_*428dup (PRC1) XP_005255044.1:n.*425_*428dup
XM_006720759.2:c.*476_*479dup (PRC1) XP_006720822.1:n.*476_*479dup
XM_006720760.2:c.1673-96_1673-93dup (PRC1) XP_006720823.1:n.1673-96_1673-93dup
XM_011522187.2:c.1792-96_1792-93dup (PRC1) XP_011520489.1:n.1792-96_1792-93dup
XM_011522188.3:c.1750-96_1750-93dup (PRC1) XP_011520490.1:n.1750-96_1750-93dup
XM_011522189.2:c.1681-96_1681-93dup (PRC1) XP_011520491.1:n.1681-96_1681-93dup
XM_011522190.3:c.1621-96_1621-93dup (PRC1) XP_011520492.1:n.1621-96_1621-93dup
XM_011522191.3:c.*23-96_*23-93dup (PRC1) XP_011520493.1:n.*23-96_*23-93dup
XM_011522192.2:c.1471-96_1471-93dup (PRC1) XP_011520494.1:n.1471-96_1471-93dup
XM_017022712.2:c.*382_*385dup (PRC1) XP_016878201.1:n.*382_*385dup
XM_017022713.2:c.*382_*385dup (PRC1) XP_016878202.1:n.*382_*385dup
XM_017022714.2:c.1636-96_1636-93dup (PRC1) XP_016878203.1:n.1636-96_1636-93dup
XM_017022715.2:c.*382_*385dup (PRC1) XP_016878204.1:n.*382_*385dup
XM_017022716.2:c.*382_*385dup (PRC1) XP_016878205.1:n.*382_*385dup
XM_017022717.1:c.*425_*428dup (PRC1) XP_016878206.1:n.*425_*428dup
NM_003981.4:c.*382_*385dup (PRC1) MANE Select NP_003972.2:n.*382_*385dup
NM_001267580.2:c.*425_*428dup (PRC1) NP_001254509.2:n.*425_*428dup
NM_199413.3:c.*382_*385dup (PRC1) NP_955445.2:n.*382_*385dup