Canonical Allele Identifier: CA2195380672

Gene: PRC1 PRC1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966597G= , CM000677.2:g.90966597G=	GRCh38
NC_000015.9:g.91509827G= , CM000677.1:g.91509827G=	GRCh37
NC_000015.8:g.89310831G=	NCBI36
NG_050647.1:g.33055C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*534C= (PRC1) MANE Select	ENSP00000377793.3:n.*534C=
ENST00000643536.1:c.*4159C=	ENSP00000494429.1:n.*4159C=
ENST00000361188.9:c.*534C= (PRC1)	ENSP00000354679.5:n.*534C=
ENST00000394249.7:c.*534C= (PRC1)	ENSP00000377793.3:n.*534C=
ENST00000555455.5:c.698C= (PRC1)
ENST00000556972.6:c.181C= (PRC1)	ENSP00000456737.1:n.181C=
NM_001267580.1:c.*577C= (PRC1)	NP_001254509.1:n.*577C=
NM_003981.3:c.*534C= (PRC1)	NP_003972.1:n.*534C=
NM_199413.2:c.*534C= (PRC1)	NP_955445.1:n.*534C=
NR_051984.1:n.229G= (PRC1-AS1)
XM_005254987.1:c.*577C= (PRC1)	XP_005255044.1:n.*577C=
XM_006720759.1:c.*628C= (PRC1)	XP_006720822.1:n.*628C=
XM_006720760.1:c.*40C= (PRC1)	XP_006720823.1:n.*40C=
XM_011522187.1:c.1848C= (PRC1)	XP_011520489.1:p.Ala616=
XM_011522188.1:c.1806C= (PRC1)	XP_011520490.1:p.Ala602=
XM_011522189.1:c.1737C= (PRC1)	XP_011520491.1:p.Ala579=
XM_011522190.1:c.1677C= (PRC1)	XP_011520492.1:p.Ala559=
XM_011522191.1:c.*79C= (PRC1)	XP_011520493.1:n.*79C=
XM_011522192.1:c.1527C= (PRC1)	XP_011520494.1:p.Ala509=
XM_005254987.3:c.*577C= (PRC1)	XP_005255044.1:n.*577C=
XM_006720759.2:c.*628C= (PRC1)	XP_006720822.1:n.*628C=
XM_006720760.2:c.*40C= (PRC1)	XP_006720823.1:n.*40C=
XM_011522187.2:c.1848C= (PRC1)	XP_011520489.1:p.Ala616=
XM_011522188.3:c.1806C= (PRC1)	XP_011520490.1:p.Ala602=
XM_011522189.2:c.1737C= (PRC1)	XP_011520491.1:p.Ala579=
XM_011522190.3:c.1677C= (PRC1)	XP_011520492.1:p.Ala559=
XM_011522191.3:c.*79C= (PRC1)	XP_011520493.1:n.*79C=
XM_011522192.2:c.1527C= (PRC1)	XP_011520494.1:p.Ala509=
XM_017022712.2:c.*534C= (PRC1)	XP_016878201.1:n.*534C=
XM_017022713.2:c.*534C= (PRC1)	XP_016878202.1:n.*534C=
XM_017022714.2:c.1692C= (PRC1)	XP_016878203.1:p.Ala564=
XM_017022715.2:c.*534C= (PRC1)	XP_016878204.1:n.*534C=
XM_017022716.2:c.*534C= (PRC1)	XP_016878205.1:n.*534C=
XM_017022717.1:c.*577C= (PRC1)	XP_016878206.1:n.*577C=
NM_003981.4:c.*534C= (PRC1) MANE Select	NP_003972.2:n.*534C=
NM_001267580.2:c.*577C= (PRC1)	NP_001254509.2:n.*577C=
NM_199413.3:c.*534C= (PRC1)	NP_955445.2:n.*534C=