Canonical Allele Identifier: CA2578756310

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373349_139373350insTGCTGCTGC , CM000668.2:g.139373349_139373350insTGCTGCTGC	GRCh38
NC_000006.11:g.139694486_139694487insTGCTGCTGC , CM000668.1:g.139694486_139694487insTGCTGCTGC	GRCh37
NC_000006.10:g.139736179_139736180insTGCTGCTGC	NCBI36
NG_016169.1:g.6302_6303insGCAGCAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.598_599insGCAGCAGCA MANE Select	ENSP00000356623.2:p.Gly199_Asn200insSerSerSer
ENST00000367651.3:c.598_599insGCAGCAGCA	ENSP00000356623.2:p.Gly199_Asn200insSerSerSer
ENST00000536159.2:c.598_599insGCAGCAGCA	ENSP00000442831.1:p.Gly199_Asn200insSerSerSer
ENST00000537332.2:c.613_614insGCAGCAGCA	ENSP00000444198.2:p.Gly204_Asn205insSerSerSer
ENST00000618718.1:c.477-50_477-49insGCAGCAGCA	ENSP00000479918.1:n.477-50_477-49insGCAGCAGCA
NM_001168388.2:c.598_599insGCAGCAGCA	NP_001161860.1:p.Gly199_Asn200insSerSerSer
NM_001168389.2:c.613_614insGCAGCAGCA	NP_001161861.2:p.Gly204_Asn205insSerSerSer
NM_006079.4:c.598_599insGCAGCAGCA	NP_006070.2:p.Gly199_Asn200insSerSerSer
NM_006079.5:c.598_599insGCAGCAGCA MANE Select	NP_006070.2:p.Gly199_Asn200insSerSerSer
NM_001168388.3:c.598_599insGCAGCAGCA	NP_001161860.1:p.Gly199_Asn200insSerSerSer
NM_001168389.3:c.613_614insGCAGCAGCA	NP_001161861.2:p.Gly204_Asn205insSerSerSer