Canonical Allele Identifier: CA619861970
Gene: PRC1 HGNC NCBI
PRC1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1567174759

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90966627_90966630dup , CM000677.2:g.90966627_90966630dup GRCh38
NC_000015.9:g.91509857_91509860dup , CM000677.1:g.91509857_91509860dup GRCh37
NC_000015.8:g.89310861_89310864dup NCBI36
NG_050647.1:g.33023_33026dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394249.8:c.*502_*505dup (PRC1) MANE Select ENSP00000377793.3:n.*502_*505dup
ENST00000643536.1:c.*4127_*4130dup ENSP00000494429.1:n.*4127_*4130dup
ENST00000361188.9:c.*502_*505dup (PRC1) ENSP00000354679.5:n.*502_*505dup
ENST00000394249.7:c.*502_*505dup (PRC1) ENSP00000377793.3:n.*502_*505dup
ENST00000555455.5:c.666_669dup (PRC1)
ENST00000556972.6:c.149_152dup (PRC1) ENSP00000456737.1:n.149_152dup
NM_001267580.1:c.*545_*548dup (PRC1) NP_001254509.1:n.*545_*548dup
NM_003981.3:c.*502_*505dup (PRC1) NP_003972.1:n.*502_*505dup
NM_199413.2:c.*502_*505dup (PRC1) NP_955445.1:n.*502_*505dup
NR_051984.1:n.259_262dup (PRC1-AS1)
XM_005254987.1:c.*545_*548dup (PRC1) XP_005255044.1:n.*545_*548dup
XM_006720759.1:c.*596_*599dup (PRC1) XP_006720822.1:n.*596_*599dup
XM_006720760.1:c.*8_*11dup (PRC1) XP_006720823.1:n.*8_*11dup
XM_011522187.1:c.1816_1819dup (PRC1) XP_011520489.1:p.Phe607CysfsTer?
XM_011522188.1:c.1774_1777dup (PRC1) XP_011520490.1:p.Phe593CysfsTer?
XM_011522189.1:c.1705_1708dup (PRC1) XP_011520491.1:p.Phe570CysfsTer?
XM_011522190.1:c.1645_1648dup (PRC1) XP_011520492.1:p.Phe550CysfsTer?
XM_011522191.1:c.*47_*50dup (PRC1) XP_011520493.1:n.*47_*50dup
XM_011522192.1:c.1495_1498dup (PRC1) XP_011520494.1:p.Phe500CysfsTer?
XM_005254987.3:c.*545_*548dup (PRC1) XP_005255044.1:n.*545_*548dup
XM_006720759.2:c.*596_*599dup (PRC1) XP_006720822.1:n.*596_*599dup
XM_006720760.2:c.*8_*11dup (PRC1) XP_006720823.1:n.*8_*11dup
XM_011522187.2:c.1816_1819dup (PRC1) XP_011520489.1:p.Phe607CysfsTer?
XM_011522188.3:c.1774_1777dup (PRC1) XP_011520490.1:p.Phe593CysfsTer?
XM_011522189.2:c.1705_1708dup (PRC1) XP_011520491.1:p.Phe570CysfsTer?
XM_011522190.3:c.1645_1648dup (PRC1) XP_011520492.1:p.Phe550CysfsTer?
XM_011522191.3:c.*47_*50dup (PRC1) XP_011520493.1:n.*47_*50dup
XM_011522192.2:c.1495_1498dup (PRC1) XP_011520494.1:p.Phe500CysfsTer?
XM_017022712.2:c.*502_*505dup (PRC1) XP_016878201.1:n.*502_*505dup
XM_017022713.2:c.*502_*505dup (PRC1) XP_016878202.1:n.*502_*505dup
XM_017022714.2:c.1660_1663dup (PRC1) XP_016878203.1:p.Phe555CysfsTer?
XM_017022715.2:c.*502_*505dup (PRC1) XP_016878204.1:n.*502_*505dup
XM_017022716.2:c.*502_*505dup (PRC1) XP_016878205.1:n.*502_*505dup
XM_017022717.1:c.*545_*548dup (PRC1) XP_016878206.1:n.*545_*548dup
NM_003981.4:c.*502_*505dup (PRC1) MANE Select NP_003972.2:n.*502_*505dup
NM_001267580.2:c.*545_*548dup (PRC1) NP_001254509.2:n.*545_*548dup
NM_199413.3:c.*502_*505dup (PRC1) NP_955445.2:n.*502_*505dup