Canonical Allele Identifier: CA1667372403

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373435_139373462delinsCGAGCCGCCGGGGGTGCTGCTGCCGCCG , CM000668.2:g.139373435_139373462delinsCGAGCCGCCGGGGGTGCTGCTGCCGCCG	GRCh38
NC_000006.11:g.139694572_139694599delinsCGAGCCGCCGGGGGTGCTGCTGCCGCCG , CM000668.1:g.139694572_139694599delinsCGAGCCGCCGGGGGTGCTGCTGCCGCCG	GRCh37
NC_000006.10:g.139736265_139736292delinsCGAGCCGCCGGGGGTGCTGCTGCCGCCG	NCBI36
NG_016169.1:g.6187_6214delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG MANE Select	ENSP00000356623.2:p.Ser161=
ENST00000367651.3:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	ENSP00000356623.2:p.Ser161=
ENST00000536159.2:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	ENSP00000442831.1:p.Ser161=
ENST00000537332.2:c.498_525delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	ENSP00000444198.2:p.Ser166=
ENST00000618718.1:c.476+7_476+34delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	ENSP00000479918.1:n.476+7_476+34delinsCGGCGGCAGCAGCACCCCCGGCG...
NM_001168388.2:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	NP_001161860.1:p.Ser161=
NM_001168389.2:c.498_525delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	NP_001161861.2:p.Ser166=
NM_006079.4:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	NP_006070.2:p.Ser161=
NM_006079.5:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG MANE Select	NP_006070.2:p.Ser161=
NM_001168388.3:c.483_510delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	NP_001161860.1:p.Ser161=
NM_001168389.3:c.498_525delinsCGGCGGCAGCAGCACCCCCGGCGGCTCG	NP_001161861.2:p.Ser166=