Canonical Allele Identifier: CA2195380587

Gene: PRC1 PRC1-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966536C= , CM000677.2:g.90966536C=	GRCh38
NC_000015.9:g.91509766C= , CM000677.1:g.91509766C=	GRCh37
NC_000015.8:g.89310770C=	NCBI36
NG_050647.1:g.33116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*595G= (PRC1) MANE Select	ENSP00000377793.3:n.*595G=
ENST00000643536.1:c.*4220G=	ENSP00000494429.1:n.*4220G=
ENST00000361188.9:c.*595G= (PRC1)	ENSP00000354679.5:n.*595G=
ENST00000394249.7:c.*595G= (PRC1)	ENSP00000377793.3:n.*595G=
ENST00000555455.5:c.759G= (PRC1)
ENST00000556972.6:c.242G= (PRC1)	ENSP00000456737.1:n.242G=
NM_001267580.1:c.*638G= (PRC1)	NP_001254509.1:n.*638G=
NM_003981.3:c.*595G= (PRC1)	NP_003972.1:n.*595G=
NM_199413.2:c.*595G= (PRC1)	NP_955445.1:n.*595G=
NR_051984.1:n.168C= (PRC1-AS1)
XM_005254987.1:c.*638G= (PRC1)	XP_005255044.1:n.*638G=
XM_006720759.1:c.*689G= (PRC1)	XP_006720822.1:n.*689G=
XM_006720760.1:c.*101G= (PRC1)	XP_006720823.1:n.*101G=
XM_011522187.1:c.*43G= (PRC1)	XP_011520489.1:n.*43G=
XM_011522188.1:c.*43G= (PRC1)	XP_011520490.1:n.*43G=
XM_011522189.1:c.*43G= (PRC1)	XP_011520491.1:n.*43G=
XM_011522190.1:c.*43G= (PRC1)	XP_011520492.1:n.*43G=
XM_011522192.1:c.*43G= (PRC1)	XP_011520494.1:n.*43G=
XM_005254987.3:c.*638G= (PRC1)	XP_005255044.1:n.*638G=
XM_006720759.2:c.*689G= (PRC1)	XP_006720822.1:n.*689G=
XM_006720760.2:c.*101G= (PRC1)	XP_006720823.1:n.*101G=
XM_011522187.2:c.*43G= (PRC1)	XP_011520489.1:n.*43G=
XM_011522188.3:c.*43G= (PRC1)	XP_011520490.1:n.*43G=
XM_011522189.2:c.*43G= (PRC1)	XP_011520491.1:n.*43G=
XM_011522190.3:c.*43G= (PRC1)	XP_011520492.1:n.*43G=
XM_011522191.3:c.*140G= (PRC1)	XP_011520493.1:n.*140G=
XM_011522192.2:c.*43G= (PRC1)	XP_011520494.1:n.*43G=
XM_017022712.2:c.*595G= (PRC1)	XP_016878201.1:n.*595G=
XM_017022713.2:c.*595G= (PRC1)	XP_016878202.1:n.*595G=
XM_017022714.2:c.*43G= (PRC1)	XP_016878203.1:n.*43G=
XM_017022715.2:c.*595G= (PRC1)	XP_016878204.1:n.*595G=
XM_017022716.2:c.*595G= (PRC1)	XP_016878205.1:n.*595G=
XM_017022717.1:c.*638G= (PRC1)	XP_016878206.1:n.*638G=
NM_003981.4:c.*595G= (PRC1) MANE Select	NP_003972.2:n.*595G=
NM_001267580.2:c.*638G= (PRC1)	NP_001254509.2:n.*638G=
NM_199413.3:c.*595G= (PRC1)	NP_955445.2:n.*595G=