Canonical Allele Identifier: CA208401

Gene: ORC4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.147935595del , CM000664.2:g.147935595del	GRCh38
NC_000002.11:g.148693164del , CM000664.1:g.148693164del	GRCh37
NC_000002.10:g.148409634del	NCBI36
NG_028252.1:g.91010del

Transcript Alleles

HGVS	Amino-acid Change
NM_181741.4:c.1226del MANE Select	NP_859525.1:p.Thr409IlefsTer4
ENST00000392857.10:c.1226del MANE Select	ENSP00000376597.5:p.Thr409IlefsTer4
NM_001190879.2:c.1226del	NP_001177808.1:p.Thr409IlefsTer4
NM_001190879.3:c.1226del	NP_001177808.1:p.Thr409IlefsTer4
NM_001190881.2:c.974del	NP_001177810.1:p.Thr325IlefsTer4
NM_001190881.3:c.974del	NP_001177810.1:p.Thr325IlefsTer4
NM_001190882.2:c.1004del	NP_001177811.1:p.Thr335IlefsTer4
NM_001190882.3:c.1004del	NP_001177811.1:p.Thr335IlefsTer4
NM_001374270.1:c.1226del	NP_001361199.1:p.Thr409IlefsTer4
NM_001374272.1:c.974del	NP_001361201.1:p.Thr325IlefsTer4
NM_002552.4:c.1226del	NP_002543.2:p.Thr409IlefsTer4
NM_002552.5:c.1226del	NP_002543.2:p.Thr409IlefsTer4
NM_181741.3:c.1226del	NP_859525.1:p.Thr409IlefsTer4
NM_181742.3:c.1226del	NP_859526.1:p.Thr409IlefsTer4
NM_181742.4:c.1226del	NP_859526.1:p.Thr409IlefsTer4
ENST00000264169.6:c.1226del	ENSP00000264169.2:p.Thr409IlefsTer4
ENST00000392857.9:c.1226del	ENSP00000376597.4:p.Thr409IlefsTer4
ENST00000535373.5:c.1226del	ENSP00000441953.1:p.Thr409IlefsTer4
ENST00000536575.5:c.974del	ENSP00000441502.1:p.Thr325IlefsTer4
ENST00000540442.5:c.1004del	ENSP00000438326.1:p.Thr335IlefsTer4
XM_006712556.2:c.974del	XP_006712619.1:p.Thr325IlefsTer4
XM_011511255.1:c.1226del	XP_011509557.1:p.Thr409IlefsTer4
XM_011511255.2:c.1226del	XP_011509557.1:p.Thr409IlefsTer4
XM_017004226.2:c.1226del	XP_016859715.1:p.Thr409IlefsTer4
XM_024452929.1:c.974del	XP_024308697.1:p.Thr325IlefsTer4