Canonical Allele Identifier: CA717052908
Gene: PRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1357676446

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966227dup , CM000677.2:g.90966227dup GRCh38
NC_000015.9:g.91509457dup , CM000677.1:g.91509457dup GRCh37
NC_000015.8:g.89310461dup NCBI36
NG_050647.1:g.33425dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*904dup MANE Select ENSP00000377793.3:n.*904dup
ENST00000643536.1:c.*4529dup ENSP00000494429.1:n.*4529dup
ENST00000361188.9:c.*904dup ENSP00000354679.5:n.*904dup
ENST00000394249.7:c.*904dup ENSP00000377793.3:n.*904dup
ENST00000556972.6:c.551dup ENSP00000456737.1:n.551dup
NM_001267580.1:c.*947dup NP_001254509.1:n.*947dup
NM_003981.3:c.*904dup NP_003972.1:n.*904dup
NM_199413.2:c.*904dup NP_955445.1:n.*904dup
XM_005254987.1:c.*947dup XP_005255044.1:n.*947dup
XM_006720759.1:c.*998dup XP_006720822.1:n.*998dup
XM_006720760.1:c.*410dup XP_006720823.1:n.*410dup
XM_011522187.1:c.*352dup XP_011520489.1:n.*352dup
XM_011522188.1:c.*352dup XP_011520490.1:n.*352dup
XM_011522189.1:c.*352dup XP_011520491.1:n.*352dup
XM_011522190.1:c.*352dup XP_011520492.1:n.*352dup
XM_011522192.1:c.*352dup XP_011520494.1:n.*352dup
XM_005254987.3:c.*947dup XP_005255044.1:n.*947dup
XM_006720759.2:c.*998dup XP_006720822.1:n.*998dup
XM_006720760.2:c.*410dup XP_006720823.1:n.*410dup
XM_011522187.2:c.*352dup XP_011520489.1:n.*352dup
XM_011522188.3:c.*352dup XP_011520490.1:n.*352dup
XM_011522189.2:c.*352dup XP_011520491.1:n.*352dup
XM_011522191.3:c.*449dup XP_011520493.1:n.*449dup
XM_011522192.2:c.*352dup XP_011520494.1:n.*352dup
XM_017022712.2:c.*904dup XP_016878201.1:n.*904dup
XM_017022713.2:c.*904dup XP_016878202.1:n.*904dup
XM_017022715.2:c.*904dup XP_016878204.1:n.*904dup
XM_017022716.2:c.*904dup XP_016878205.1:n.*904dup
XM_017022717.1:c.*947dup XP_016878206.1:n.*947dup
NM_003981.4:c.*904dup MANE Select NP_003972.2:n.*904dup
NM_001267580.2:c.*947dup NP_001254509.2:n.*947dup
NM_199413.3:c.*904dup NP_955445.2:n.*904dup