Canonical Allele Identifier: CA1899680

Gene: ORC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147958859T>G , CM000664.2:g.147958859T>G	GRCh38
NC_000002.11:g.148716428T>G , CM000664.1:g.148716428T>G	GRCh37
NC_000002.10:g.148432898T>G	NCBI36
NG_028252.1:g.67746A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392857.10:c.233A>C MANE Select	ENSP00000376597.5:p.Asn78Thr
ENST00000264169.6:c.233A>C	ENSP00000264169.2:p.Asn78Thr
ENST00000392857.9:c.233A>C	ENSP00000376597.4:p.Asn78Thr
ENST00000416719.5:c.233A>C	ENSP00000413939.1:p.Asn78Thr
ENST00000440042.1:c.233A>C	ENSP00000403105.1:p.Asn78Thr
ENST00000457954.5:c.233A>C	ENSP00000391484.1:p.Asn78Thr
ENST00000461711.5:n.137A>C
ENST00000490200.5:n.307A>C
ENST00000495601.1:n.344A>C
ENST00000496670.6:n.99A>C
ENST00000535373.5:c.233A>C	ENSP00000441953.1:p.Asn78Thr
ENST00000536575.5:c.-20A>C	ENSP00000441502.1:n.-20A>C
ENST00000540442.5:c.11A>C	ENSP00000438326.1:p.Asn4Thr
NM_001190879.2:c.233A>C	NP_001177808.1:p.Asn78Thr
NM_001190881.2:c.-20A>C	NP_001177810.1:n.-20A>C
NM_001190882.2:c.11A>C	NP_001177811.1:p.Asn4Thr
NM_002552.4:c.233A>C	NP_002543.2:p.Asn78Thr
NM_181741.3:c.233A>C	NP_859525.1:p.Asn78Thr
NM_181742.3:c.233A>C	NP_859526.1:p.Asn78Thr
XM_006712556.2:c.-20A>C	XP_006712619.1:n.-20A>C
XM_011511255.1:c.233A>C	XP_011509557.1:p.Asn78Thr
XM_011511255.2:c.233A>C	XP_011509557.1:p.Asn78Thr
XM_017004226.2:c.233A>C	XP_016859715.1:p.Asn78Thr
XM_024452929.1:c.-20A>C	XP_024308697.1:n.-20A>C
NM_001374270.1:c.233A>C	NP_001361199.1:p.Asn78Thr
NM_001374272.1:c.-20A>C	NP_001361201.1:n.-20A>C
NM_002552.5:c.233A>C	NP_002543.2:p.Asn78Thr
NM_181741.4:c.233A>C MANE Select	NP_859525.1:p.Asn78Thr
NM_001190879.3:c.233A>C	NP_001177808.1:p.Asn78Thr
NM_001190881.3:c.-20A>C	NP_001177810.1:n.-20A>C
NM_001190882.3:c.11A>C	NP_001177811.1:p.Asn4Thr
NM_181742.4:c.233A>C	NP_859526.1:p.Asn78Thr