Canonical Allele Identifier: CA1667372339

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373356_139373374delinsCGCTGCCGCCGCCGCTGTT , CM000668.2:g.139373356_139373374delinsCGCTGCCGCCGCCGCTGTT	GRCh38
NC_000006.11:g.139694493_139694511delinsCGCTGCCGCCGCCGCTGTT , CM000668.1:g.139694493_139694511delinsCGCTGCCGCCGCCGCTGTT	GRCh37
NC_000006.10:g.139736186_139736204delinsCGCTGCCGCCGCCGCTGTT	NCBI36
NG_016169.1:g.6275_6293delinsAACAGCGGCGGCGGCAGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.571_589delinsAACAGCGGCGGCGGCAGCG MANE Select	ENSP00000356623.2:p.Asn191=
ENST00000367651.3:c.571_589delinsAACAGCGGCGGCGGCAGCG	ENSP00000356623.2:p.Asn191=
ENST00000536159.2:c.571_589delinsAACAGCGGCGGCGGCAGCG	ENSP00000442831.1:p.Asn191=
ENST00000537332.2:c.586_604delinsAACAGCGGCGGCGGCAGCG	ENSP00000444198.2:p.Asn196=
ENST00000618718.1:c.477-77_477-59delinsAACAGCGGCGGCGGCAGCG	ENSP00000479918.1:n.477-77_477-59delinsAACAGCGGCGGCGGCAGCG
NM_001168388.2:c.571_589delinsAACAGCGGCGGCGGCAGCG	NP_001161860.1:p.Asn191=
NM_001168389.2:c.586_604delinsAACAGCGGCGGCGGCAGCG	NP_001161861.2:p.Asn196=
NM_006079.4:c.571_589delinsAACAGCGGCGGCGGCAGCG	NP_006070.2:p.Asn191=
NM_006079.5:c.571_589delinsAACAGCGGCGGCGGCAGCG MANE Select	NP_006070.2:p.Asn191=
NM_001168388.3:c.571_589delinsAACAGCGGCGGCGGCAGCG	NP_001161860.1:p.Asn191=
NM_001168389.3:c.586_604delinsAACAGCGGCGGCGGCAGCG	NP_001161861.2:p.Asn196=