Canonical Allele Identifier: CA2195381189

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966361A= , CM000677.2:g.90966361A=	GRCh38
NC_000015.9:g.91509591A= , CM000677.1:g.91509591A=	GRCh37
NC_000015.8:g.89310595A=	NCBI36
NG_050647.1:g.33291T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*770T= MANE Select	ENSP00000377793.3:n.*770T=
ENST00000643536.1:c.*4395T=	ENSP00000494429.1:n.*4395T=
ENST00000361188.9:c.*770T=	ENSP00000354679.5:n.*770T=
ENST00000394249.7:c.*770T=	ENSP00000377793.3:n.*770T=
ENST00000556972.6:c.417T=	ENSP00000456737.1:n.417T=
NM_001267580.1:c.*813T=	NP_001254509.1:n.*813T=
NM_003981.3:c.*770T=	NP_003972.1:n.*770T=
NM_199413.2:c.*770T=	NP_955445.1:n.*770T=
XM_005254987.1:c.*813T=	XP_005255044.1:n.*813T=
XM_006720759.1:c.*864T=	XP_006720822.1:n.*864T=
XM_006720760.1:c.*276T=	XP_006720823.1:n.*276T=
XM_011522187.1:c.*218T=	XP_011520489.1:n.*218T=
XM_011522188.1:c.*218T=	XP_011520490.1:n.*218T=
XM_011522189.1:c.*218T=	XP_011520491.1:n.*218T=
XM_011522190.1:c.*218T=	XP_011520492.1:n.*218T=
XM_011522192.1:c.*218T=	XP_011520494.1:n.*218T=
XM_005254987.3:c.*813T=	XP_005255044.1:n.*813T=
XM_006720759.2:c.*864T=	XP_006720822.1:n.*864T=
XM_006720760.2:c.*276T=	XP_006720823.1:n.*276T=
XM_011522187.2:c.*218T=	XP_011520489.1:n.*218T=
XM_011522188.3:c.*218T=	XP_011520490.1:n.*218T=
XM_011522189.2:c.*218T=	XP_011520491.1:n.*218T=
XM_011522191.3:c.*315T=	XP_011520493.1:n.*315T=
XM_011522192.2:c.*218T=	XP_011520494.1:n.*218T=
XM_017022712.2:c.*770T=	XP_016878201.1:n.*770T=
XM_017022713.2:c.*770T=	XP_016878202.1:n.*770T=
XM_017022715.2:c.*770T=	XP_016878204.1:n.*770T=
XM_017022716.2:c.*770T=	XP_016878205.1:n.*770T=
XM_017022717.1:c.*813T=	XP_016878206.1:n.*813T=
NM_003981.4:c.*770T= MANE Select	NP_003972.2:n.*770T=
NM_001267580.2:c.*813T=	NP_001254509.2:n.*813T=
NM_199413.3:c.*770T=	NP_955445.2:n.*770T=