Canonical Allele Identifier: CA1644643613

Gene: ORC3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87667331T= , CM000668.2:g.87667331T=	GRCh38
NC_000006.11:g.88377049T= , CM000668.1:g.88377049T=	GRCh37
NC_000006.10:g.88433768T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392844.8:c.*208T= MANE Select	ENSP00000376586.3:n.*208T=
ENST00000257789.4:c.*208T=	ENSP00000257789.4:n.*208T=
ENST00000392844.7:c.*208T=	ENSP00000376586.3:n.*208T=
ENST00000546266.5:c.*208T=	ENSP00000444695.1:n.*208T=
NM_001197259.1:c.*208T=	NP_001184188.1:n.*208T=
NM_012381.3:c.*208T=	NP_036513.2:n.*208T=
NM_181837.2:c.*208T=	NP_862820.1:n.*208T=
XM_005248704.1:c.*299T=	XP_005248761.1:n.*299T=
XM_005248705.1:c.*208T=	XP_005248762.1:n.*208T=
XM_005248706.1:c.*208T=	XP_005248763.1:n.*208T=
XM_011535651.1:c.*208T=	XP_011533953.1:n.*208T=
XM_005248704.2:c.*299T=	XP_005248761.1:n.*299T=
XM_005248705.2:c.*208T=	XP_005248762.1:n.*208T=
XM_011535651.2:c.*208T=	XP_011533953.1:n.*208T=
XM_017010632.2:c.2033+1498T=	XP_016866121.1:n.2033+1498T=
XM_017010633.2:c.2030+1498T=	XP_016866122.1:n.2030+1498T=
XM_017010634.2:c.*299T=	XP_016866123.1:n.*299T=
XM_017010635.2:c.*208T=	XP_016866124.1:n.*208T=
XM_017010636.2:c.*208T=	XP_016866125.1:n.*208T=
XM_017010637.1:c.*208T=	XP_016866126.1:n.*208T=
XM_017010638.2:c.*299T=	XP_016866127.1:n.*299T=
XM_017010639.1:c.*299T=	XP_016866128.1:n.*299T=
XM_017010640.1:c.*208T=	XP_016866129.1:n.*208T=
XR_001743294.2:n.2441T=
XR_001743295.2:n.2438T=
NM_001197259.2:c.*208T=	NP_001184188.1:n.*208T=
NM_012381.4:c.*208T= MANE Select	NP_036513.2:n.*208T=
NM_181837.3:c.*208T=	NP_862820.1:n.*208T=