Canonical Allele Identifier: CA1667372324

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373343_139373370delinsATGTTGCCGCTGCCGCTGCCGCCGCCGC , CM000668.2:g.139373343_139373370delinsATGTTGCCGCTGCCGCTGCCGCCGCCGC	GRCh38
NC_000006.11:g.139694480_139694507delinsATGTTGCCGCTGCCGCTGCCGCCGCCGC , CM000668.1:g.139694480_139694507delinsATGTTGCCGCTGCCGCTGCCGCCGCCGC	GRCh37
NC_000006.10:g.139736173_139736200delinsATGTTGCCGCTGCCGCTGCCGCCGCCGC	NCBI36
NG_016169.1:g.6279_6306delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT MANE Select	ENSP00000356623.2:p.Ser192=
ENST00000367651.3:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	ENSP00000356623.2:p.Ser192=
ENST00000536159.2:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	ENSP00000442831.1:p.Ser192=
ENST00000537332.2:c.590_617delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	ENSP00000444198.2:p.Ser197=
ENST00000618718.1:c.477-73_477-46delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	ENSP00000479918.1:n.477-73_477-46delinsGCGGCGGCGGCAGCGGCAGCGG...
NM_001168388.2:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	NP_001161860.1:p.Ser192=
NM_001168389.2:c.590_617delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	NP_001161861.2:p.Ser197=
NM_006079.4:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	NP_006070.2:p.Ser192=
NM_006079.5:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT MANE Select	NP_006070.2:p.Ser192=
NM_001168388.3:c.575_602delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	NP_001161860.1:p.Ser192=
NM_001168389.3:c.590_617delinsGCGGCGGCGGCAGCGGCAGCGGCAACAT	NP_001161861.2:p.Ser197=