Canonical Allele Identifier: CA2195380728

Gene: PRC1 PRC1-AS1

Linked Data

• dbSNP Id: rs2037514176

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966643_90966644dup , CM000677.2:g.90966643_90966644dup	GRCh38
NC_000015.9:g.91509873_91509874dup , CM000677.1:g.91509873_91509874dup	GRCh37
NC_000015.8:g.89310877_89310878dup	NCBI36
NG_050647.1:g.33008_33009dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*487_*488dup (PRC1) MANE Select	ENSP00000377793.3:n.*487_*488dup
ENST00000643536.1:c.*4112_*4113dup	ENSP00000494429.1:n.*4112_*4113dup
ENST00000361188.9:c.*487_*488dup (PRC1)	ENSP00000354679.5:n.*487_*488dup
ENST00000394249.7:c.*487_*488dup (PRC1)	ENSP00000377793.3:n.*487_*488dup
ENST00000555455.5:c.651_652dup (PRC1)
ENST00000556972.6:c.134_135dup (PRC1)	ENSP00000456737.1:p.Ser46ProfsTer22
NM_001267580.1:c.*530_*531dup (PRC1)	NP_001254509.1:n.*530_*531dup
NM_003981.3:c.*487_*488dup (PRC1)	NP_003972.1:n.*487_*488dup
NM_199413.2:c.*487_*488dup (PRC1)	NP_955445.1:n.*487_*488dup
NR_051984.1:n.275_276dup (PRC1-AS1)
XM_005254987.1:c.*530_*531dup (PRC1)	XP_005255044.1:n.*530_*531dup
XM_006720759.1:c.*581_*582dup (PRC1)	XP_006720822.1:n.*581_*582dup
XM_006720760.1:c.1682_1683dup (PRC1)	XP_006720823.1:p.Ser562ProfsTer22
XM_011522187.1:c.1801_1802dup (PRC1)	XP_011520489.1:p.Pro602LeufsTer12
XM_011522188.1:c.1759_1760dup (PRC1)	XP_011520490.1:p.Pro588LeufsTer12
XM_011522189.1:c.1690_1691dup (PRC1)	XP_011520491.1:p.Pro565LeufsTer12
XM_011522190.1:c.1630_1631dup (PRC1)	XP_011520492.1:p.Pro545LeufsTer12
XM_011522191.1:c.*32_*33dup (PRC1)	XP_011520493.1:n.*32_*33dup
XM_011522192.1:c.1480_1481dup (PRC1)	XP_011520494.1:p.Pro495LeufsTer12
XM_005254987.3:c.*530_*531dup (PRC1)	XP_005255044.1:n.*530_*531dup
XM_006720759.2:c.*581_*582dup (PRC1)	XP_006720822.1:n.*581_*582dup
XM_006720760.2:c.1682_1683dup (PRC1)	XP_006720823.1:p.Ser562ProfsTer22
XM_011522187.2:c.1801_1802dup (PRC1)	XP_011520489.1:p.Pro602LeufsTer12
XM_011522188.3:c.1759_1760dup (PRC1)	XP_011520490.1:p.Pro588LeufsTer12
XM_011522189.2:c.1690_1691dup (PRC1)	XP_011520491.1:p.Pro565LeufsTer12
XM_011522190.3:c.1630_1631dup (PRC1)	XP_011520492.1:p.Pro545LeufsTer12
XM_011522191.3:c.*32_*33dup (PRC1)	XP_011520493.1:n.*32_*33dup
XM_011522192.2:c.1480_1481dup (PRC1)	XP_011520494.1:p.Pro495LeufsTer12
XM_017022712.2:c.*487_*488dup (PRC1)	XP_016878201.1:n.*487_*488dup
XM_017022713.2:c.*487_*488dup (PRC1)	XP_016878202.1:n.*487_*488dup
XM_017022714.2:c.1645_1646dup (PRC1)	XP_016878203.1:p.Pro550LeufsTer12
XM_017022715.2:c.*487_*488dup (PRC1)	XP_016878204.1:n.*487_*488dup
XM_017022716.2:c.*487_*488dup (PRC1)	XP_016878205.1:n.*487_*488dup
XM_017022717.1:c.*530_*531dup (PRC1)	XP_016878206.1:n.*530_*531dup
NM_003981.4:c.*487_*488dup (PRC1) MANE Select	NP_003972.2:n.*487_*488dup
NM_001267580.2:c.*530_*531dup (PRC1)	NP_001254509.2:n.*530_*531dup
NM_199413.3:c.*487_*488dup (PRC1)	NP_955445.2:n.*487_*488dup