Canonical Allele Identifier: CA2195380703
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966624A= , CM000677.2:g.90966624A= GRCh38
NC_000015.9:g.91509854A= , CM000677.1:g.91509854A= GRCh37
NC_000015.8:g.89310858A= NCBI36
NG_050647.1:g.33028T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*507T= (PRC1) MANE Select ENSP00000377793.3:n.*507T=
ENST00000643536.1:c.*4132T= ENSP00000494429.1:n.*4132T=
ENST00000361188.9:c.*507T= (PRC1) ENSP00000354679.5:n.*507T=
ENST00000394249.7:c.*507T= (PRC1) ENSP00000377793.3:n.*507T=
ENST00000555455.5:c.671T= (PRC1)
ENST00000556972.6:c.154T= (PRC1) ENSP00000456737.1:n.154T=
NM_001267580.1:c.*550T= (PRC1) NP_001254509.1:n.*550T=
NM_003981.3:c.*507T= (PRC1) NP_003972.1:n.*507T=
NM_199413.2:c.*507T= (PRC1) NP_955445.1:n.*507T=
NR_051984.1:n.256A= (PRC1-AS1)
XM_005254987.1:c.*550T= (PRC1) XP_005255044.1:n.*550T=
XM_006720759.1:c.*601T= (PRC1) XP_006720822.1:n.*601T=
XM_006720760.1:c.*13T= (PRC1) XP_006720823.1:n.*13T=
XM_011522187.1:c.1821T= (PRC1) XP_011520489.1:p.Phe607=
XM_011522188.1:c.1779T= (PRC1) XP_011520490.1:p.Phe593=
XM_011522189.1:c.1710T= (PRC1) XP_011520491.1:p.Phe570=
XM_011522190.1:c.1650T= (PRC1) XP_011520492.1:p.Phe550=
XM_011522191.1:c.*52T= (PRC1) XP_011520493.1:n.*52T=
XM_011522192.1:c.1500T= (PRC1) XP_011520494.1:p.Phe500=
XM_005254987.3:c.*550T= (PRC1) XP_005255044.1:n.*550T=
XM_006720759.2:c.*601T= (PRC1) XP_006720822.1:n.*601T=
XM_006720760.2:c.*13T= (PRC1) XP_006720823.1:n.*13T=
XM_011522187.2:c.1821T= (PRC1) XP_011520489.1:p.Phe607=
XM_011522188.3:c.1779T= (PRC1) XP_011520490.1:p.Phe593=
XM_011522189.2:c.1710T= (PRC1) XP_011520491.1:p.Phe570=
XM_011522190.3:c.1650T= (PRC1) XP_011520492.1:p.Phe550=
XM_011522191.3:c.*52T= (PRC1) XP_011520493.1:n.*52T=
XM_011522192.2:c.1500T= (PRC1) XP_011520494.1:p.Phe500=
XM_017022712.2:c.*507T= (PRC1) XP_016878201.1:n.*507T=
XM_017022713.2:c.*507T= (PRC1) XP_016878202.1:n.*507T=
XM_017022714.2:c.1665T= (PRC1) XP_016878203.1:p.Phe555=
XM_017022715.2:c.*507T= (PRC1) XP_016878204.1:n.*507T=
XM_017022716.2:c.*507T= (PRC1) XP_016878205.1:n.*507T=
XM_017022717.1:c.*550T= (PRC1) XP_016878206.1:n.*550T=
NM_003981.4:c.*507T= (PRC1) MANE Select NP_003972.2:n.*507T=
NM_001267580.2:c.*550T= (PRC1) NP_001254509.2:n.*550T=
NM_199413.3:c.*507T= (PRC1) NP_955445.2:n.*507T=