Canonical Allele Identifier: CA1667372329

Gene: CITED2

Linked Data

• dbSNP Id: rs1778293007

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373349_139373350insTGCCGC , CM000668.2:g.139373349_139373350insTGCCGC	GRCh38
NC_000006.11:g.139694486_139694487insTGCCGC , CM000668.1:g.139694486_139694487insTGCCGC	GRCh37
NC_000006.10:g.139736179_139736180insTGCCGC	NCBI36
NG_016169.1:g.6301_6302insGGCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.597_598insGGCAGC MANE Select	ENSP00000356623.2:p.Gly199_Asn200insGlySer
ENST00000367651.3:c.597_598insGGCAGC	ENSP00000356623.2:p.Gly199_Asn200insGlySer
ENST00000536159.2:c.597_598insGGCAGC	ENSP00000442831.1:p.Gly199_Asn200insGlySer
ENST00000537332.2:c.612_613insGGCAGC	ENSP00000444198.2:p.Gly204_Asn205insGlySer
ENST00000618718.1:c.477-51_477-50insGGCAGC	ENSP00000479918.1:n.477-51_477-50insGGCAGC
NM_001168388.2:c.597_598insGGCAGC	NP_001161860.1:p.Gly199_Asn200insGlySer
NM_001168389.2:c.612_613insGGCAGC	NP_001161861.2:p.Gly204_Asn205insGlySer
NM_006079.4:c.597_598insGGCAGC	NP_006070.2:p.Gly199_Asn200insGlySer
NM_006079.5:c.597_598insGGCAGC MANE Select	NP_006070.2:p.Gly199_Asn200insGlySer
NM_001168388.3:c.597_598insGGCAGC	NP_001161860.1:p.Gly199_Asn200insGlySer
NM_001168389.3:c.612_613insGGCAGC	NP_001161861.2:p.Gly204_Asn205insGlySer