Canonical Allele Identifier: CA2195381178

Gene: PRC1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90966357A= , CM000677.2:g.90966357A=	GRCh38
NC_000015.9:g.91509587A= , CM000677.1:g.91509587A=	GRCh37
NC_000015.8:g.89310591A=	NCBI36
NG_050647.1:g.33295T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394249.8:c.*774T= MANE Select	ENSP00000377793.3:n.*774T=
ENST00000643536.1:c.*4399T=	ENSP00000494429.1:n.*4399T=
ENST00000361188.9:c.*774T=	ENSP00000354679.5:n.*774T=
ENST00000394249.7:c.*774T=	ENSP00000377793.3:n.*774T=
ENST00000556972.6:c.421T=	ENSP00000456737.1:n.421T=
NM_001267580.1:c.*817T=	NP_001254509.1:n.*817T=
NM_003981.3:c.*774T=	NP_003972.1:n.*774T=
NM_199413.2:c.*774T=	NP_955445.1:n.*774T=
XM_005254987.1:c.*817T=	XP_005255044.1:n.*817T=
XM_006720759.1:c.*868T=	XP_006720822.1:n.*868T=
XM_006720760.1:c.*280T=	XP_006720823.1:n.*280T=
XM_011522187.1:c.*222T=	XP_011520489.1:n.*222T=
XM_011522188.1:c.*222T=	XP_011520490.1:n.*222T=
XM_011522189.1:c.*222T=	XP_011520491.1:n.*222T=
XM_011522190.1:c.*222T=	XP_011520492.1:n.*222T=
XM_011522192.1:c.*222T=	XP_011520494.1:n.*222T=
XM_005254987.3:c.*817T=	XP_005255044.1:n.*817T=
XM_006720759.2:c.*868T=	XP_006720822.1:n.*868T=
XM_006720760.2:c.*280T=	XP_006720823.1:n.*280T=
XM_011522187.2:c.*222T=	XP_011520489.1:n.*222T=
XM_011522188.3:c.*222T=	XP_011520490.1:n.*222T=
XM_011522189.2:c.*222T=	XP_011520491.1:n.*222T=
XM_011522191.3:c.*319T=	XP_011520493.1:n.*319T=
XM_011522192.2:c.*222T=	XP_011520494.1:n.*222T=
XM_017022712.2:c.*774T=	XP_016878201.1:n.*774T=
XM_017022713.2:c.*774T=	XP_016878202.1:n.*774T=
XM_017022715.2:c.*774T=	XP_016878204.1:n.*774T=
XM_017022716.2:c.*774T=	XP_016878205.1:n.*774T=
XM_017022717.1:c.*817T=	XP_016878206.1:n.*817T=
NM_003981.4:c.*774T= MANE Select	NP_003972.2:n.*774T=
NM_001267580.2:c.*817T=	NP_001254509.2:n.*817T=
NM_199413.3:c.*774T=	NP_955445.2:n.*774T=