Canonical Allele Identifier: CA2630415259

Gene: PRC1 PRC1-AS1

Linked Data

• gnomAD v4: 15-90966646-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966648dup , CM000677.2:g.90966648dup	GRCh38
NC_000015.9:g.91509878dup , CM000677.1:g.91509878dup	GRCh37
NC_000015.8:g.89310882dup	NCBI36
NG_050647.1:g.33005dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*484dup (PRC1) MANE Select	ENSP00000377793.3:n.*484dup
ENST00000643536.1:c.*4109dup	ENSP00000494429.1:n.*4109dup
ENST00000361188.9:c.*484dup (PRC1)	ENSP00000354679.5:n.*484dup
ENST00000394249.7:c.*484dup (PRC1)	ENSP00000377793.3:n.*484dup
ENST00000555455.5:c.648dup (PRC1)
ENST00000556972.6:c.131dup (PRC1)	ENSP00000456737.1:p.Ser45PhefsTer13
NM_001267580.1:c.*527dup (PRC1)	NP_001254509.1:n.*527dup
NM_003981.3:c.*484dup (PRC1)	NP_003972.1:n.*484dup
NM_199413.2:c.*484dup (PRC1)	NP_955445.1:n.*484dup
NR_051984.1:n.280dup (PRC1-AS1)
XM_005254987.1:c.*527dup (PRC1)	XP_005255044.1:n.*527dup
XM_006720759.1:c.*578dup (PRC1)	XP_006720822.1:n.*578dup
XM_006720760.1:c.1679dup (PRC1)	XP_006720823.1:p.Ser561PhefsTer13
XM_011522187.1:c.1798dup (PRC1)	XP_011520489.1:p.Leu600ProfsTer4
XM_011522188.1:c.1756dup (PRC1)	XP_011520490.1:p.Leu586ProfsTer4
XM_011522189.1:c.1687dup (PRC1)	XP_011520491.1:p.Leu563ProfsTer4
XM_011522190.1:c.1627dup (PRC1)	XP_011520492.1:p.Leu543ProfsTer4
XM_011522191.1:c.*29dup (PRC1)	XP_011520493.1:n.*29dup
XM_011522192.1:c.1477dup (PRC1)	XP_011520494.1:p.Leu493ProfsTer4
XM_005254987.3:c.*527dup (PRC1)	XP_005255044.1:n.*527dup
XM_006720759.2:c.*578dup (PRC1)	XP_006720822.1:n.*578dup
XM_006720760.2:c.1679dup (PRC1)	XP_006720823.1:p.Ser561PhefsTer13
XM_011522187.2:c.1798dup (PRC1)	XP_011520489.1:p.Leu600ProfsTer4
XM_011522188.3:c.1756dup (PRC1)	XP_011520490.1:p.Leu586ProfsTer4
XM_011522189.2:c.1687dup (PRC1)	XP_011520491.1:p.Leu563ProfsTer4
XM_011522190.3:c.1627dup (PRC1)	XP_011520492.1:p.Leu543ProfsTer4
XM_011522191.3:c.*29dup (PRC1)	XP_011520493.1:n.*29dup
XM_011522192.2:c.1477dup (PRC1)	XP_011520494.1:p.Leu493ProfsTer4
XM_017022712.2:c.*484dup (PRC1)	XP_016878201.1:n.*484dup
XM_017022713.2:c.*484dup (PRC1)	XP_016878202.1:n.*484dup
XM_017022714.2:c.1642dup (PRC1)	XP_016878203.1:p.Leu548ProfsTer4
XM_017022715.2:c.*484dup (PRC1)	XP_016878204.1:n.*484dup
XM_017022716.2:c.*484dup (PRC1)	XP_016878205.1:n.*484dup
XM_017022717.1:c.*527dup (PRC1)	XP_016878206.1:n.*527dup
NM_003981.4:c.*484dup (PRC1) MANE Select	NP_003972.2:n.*484dup
NM_001267580.2:c.*527dup (PRC1)	NP_001254509.2:n.*527dup
NM_199413.3:c.*484dup (PRC1)	NP_955445.2:n.*484dup