Canonical Allele Identifier: CA2195380700
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966623C= , CM000677.2:g.90966623C= GRCh38
NC_000015.9:g.91509853C= , CM000677.1:g.91509853C= GRCh37
NC_000015.8:g.89310857C= NCBI36
NG_050647.1:g.33029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*508G= (PRC1) MANE Select ENSP00000377793.3:n.*508G=
ENST00000643536.1:c.*4133G= ENSP00000494429.1:n.*4133G=
ENST00000361188.9:c.*508G= (PRC1) ENSP00000354679.5:n.*508G=
ENST00000394249.7:c.*508G= (PRC1) ENSP00000377793.3:n.*508G=
ENST00000555455.5:c.672G= (PRC1)
ENST00000556972.6:c.155G= (PRC1) ENSP00000456737.1:n.155G=
NM_001267580.1:c.*551G= (PRC1) NP_001254509.1:n.*551G=
NM_003981.3:c.*508G= (PRC1) NP_003972.1:n.*508G=
NM_199413.2:c.*508G= (PRC1) NP_955445.1:n.*508G=
NR_051984.1:n.255C= (PRC1-AS1)
XM_005254987.1:c.*551G= (PRC1) XP_005255044.1:n.*551G=
XM_006720759.1:c.*602G= (PRC1) XP_006720822.1:n.*602G=
XM_006720760.1:c.*14G= (PRC1) XP_006720823.1:n.*14G=
XM_011522187.1:c.1822G= (PRC1) XP_011520489.1:p.Val608=
XM_011522188.1:c.1780G= (PRC1) XP_011520490.1:p.Val594=
XM_011522189.1:c.1711G= (PRC1) XP_011520491.1:p.Val571=
XM_011522190.1:c.1651G= (PRC1) XP_011520492.1:p.Val551=
XM_011522191.1:c.*53G= (PRC1) XP_011520493.1:n.*53G=
XM_011522192.1:c.1501G= (PRC1) XP_011520494.1:p.Val501=
XM_005254987.3:c.*551G= (PRC1) XP_005255044.1:n.*551G=
XM_006720759.2:c.*602G= (PRC1) XP_006720822.1:n.*602G=
XM_006720760.2:c.*14G= (PRC1) XP_006720823.1:n.*14G=
XM_011522187.2:c.1822G= (PRC1) XP_011520489.1:p.Val608=
XM_011522188.3:c.1780G= (PRC1) XP_011520490.1:p.Val594=
XM_011522189.2:c.1711G= (PRC1) XP_011520491.1:p.Val571=
XM_011522190.3:c.1651G= (PRC1) XP_011520492.1:p.Val551=
XM_011522191.3:c.*53G= (PRC1) XP_011520493.1:n.*53G=
XM_011522192.2:c.1501G= (PRC1) XP_011520494.1:p.Val501=
XM_017022712.2:c.*508G= (PRC1) XP_016878201.1:n.*508G=
XM_017022713.2:c.*508G= (PRC1) XP_016878202.1:n.*508G=
XM_017022714.2:c.1666G= (PRC1) XP_016878203.1:p.Val556=
XM_017022715.2:c.*508G= (PRC1) XP_016878204.1:n.*508G=
XM_017022716.2:c.*508G= (PRC1) XP_016878205.1:n.*508G=
XM_017022717.1:c.*551G= (PRC1) XP_016878206.1:n.*551G=
NM_003981.4:c.*508G= (PRC1) MANE Select NP_003972.2:n.*508G=
NM_001267580.2:c.*551G= (PRC1) NP_001254509.2:n.*551G=
NM_199413.3:c.*508G= (PRC1) NP_955445.2:n.*508G=