Canonical Allele Identifier: CA2195380702

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037511142

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966625_90966626del , CM000677.2:g.90966625_90966626del	GRCh38
NC_000015.9:g.91509855_91509856del , CM000677.1:g.91509855_91509856del	GRCh37
NC_000015.8:g.89310859_89310860del	NCBI36
NG_050647.1:g.33027_33028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*506_*507del (PRC1) MANE Select	ENSP00000377793.3:n.*506_*507del
ENST00000643536.1:c.*4131_*4132del	ENSP00000494429.1:n.*4131_*4132del
ENST00000361188.9:c.*506_*507del (PRC1)	ENSP00000354679.5:n.*506_*507del
ENST00000394249.7:c.*506_*507del (PRC1)	ENSP00000377793.3:n.*506_*507del
ENST00000555455.5:c.670_671del (PRC1)
ENST00000556972.6:c.153_154del (PRC1)	ENSP00000456737.1:n.153_154del
NM_001267580.1:c.*549_*550del (PRC1)	NP_001254509.1:n.*549_*550del
NM_003981.3:c.*506_*507del (PRC1)	NP_003972.1:n.*506_*507del
NM_199413.2:c.*506_*507del (PRC1)	NP_955445.1:n.*506_*507del
NR_051984.1:n.257_258del (PRC1-AS1)
XM_005254987.1:c.*549_*550del (PRC1)	XP_005255044.1:n.*549_*550del
XM_006720759.1:c.*600_*601del (PRC1)	XP_006720822.1:n.*600_*601del
XM_006720760.1:c.*12_*13del (PRC1)	XP_006720823.1:n.*12_*13del
XM_011522187.1:c.1820_1821del (PRC1)	XP_011520489.1:p.Phe607CysfsTer?
XM_011522188.1:c.1778_1779del (PRC1)	XP_011520490.1:p.Phe593CysfsTer?
XM_011522189.1:c.1709_1710del (PRC1)	XP_011520491.1:p.Phe570CysfsTer?
XM_011522190.1:c.1649_1650del (PRC1)	XP_011520492.1:p.Phe550CysfsTer?
XM_011522191.1:c.*51_*52del (PRC1)	XP_011520493.1:n.*51_*52del
XM_011522192.1:c.1499_1500del (PRC1)	XP_011520494.1:p.Phe500CysfsTer?
XM_005254987.3:c.*549_*550del (PRC1)	XP_005255044.1:n.*549_*550del
XM_006720759.2:c.*600_*601del (PRC1)	XP_006720822.1:n.*600_*601del
XM_006720760.2:c.*12_*13del (PRC1)	XP_006720823.1:n.*12_*13del
XM_011522187.2:c.1820_1821del (PRC1)	XP_011520489.1:p.Phe607CysfsTer?
XM_011522188.3:c.1778_1779del (PRC1)	XP_011520490.1:p.Phe593CysfsTer?
XM_011522189.2:c.1709_1710del (PRC1)	XP_011520491.1:p.Phe570CysfsTer?
XM_011522190.3:c.1649_1650del (PRC1)	XP_011520492.1:p.Phe550CysfsTer?
XM_011522191.3:c.*51_*52del (PRC1)	XP_011520493.1:n.*51_*52del
XM_011522192.2:c.1499_1500del (PRC1)	XP_011520494.1:p.Phe500CysfsTer?
XM_017022712.2:c.*506_*507del (PRC1)	XP_016878201.1:n.*506_*507del
XM_017022713.2:c.*506_*507del (PRC1)	XP_016878202.1:n.*506_*507del
XM_017022714.2:c.1664_1665del (PRC1)	XP_016878203.1:p.Phe555CysfsTer?
XM_017022715.2:c.*506_*507del (PRC1)	XP_016878204.1:n.*506_*507del
XM_017022716.2:c.*506_*507del (PRC1)	XP_016878205.1:n.*506_*507del
XM_017022717.1:c.*549_*550del (PRC1)	XP_016878206.1:n.*549_*550del
NM_003981.4:c.*506_*507del (PRC1) MANE Select	NP_003972.2:n.*506_*507del
NM_001267580.2:c.*549_*550del (PRC1)	NP_001254509.2:n.*549_*550del
NM_199413.3:c.*506_*507del (PRC1)	NP_955445.2:n.*506_*507del