Canonical Allele Identifier: CA1667372387

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373408_139373435delinsAGAGCCGCCGGGGGTGCTGCTGCCGCCC , CM000668.2:g.139373408_139373435delinsAGAGCCGCCGGGGGTGCTGCTGCCGCCC	GRCh38
NC_000006.11:g.139694545_139694572delinsAGAGCCGCCGGGGGTGCTGCTGCCGCCC , CM000668.1:g.139694545_139694572delinsAGAGCCGCCGGGGGTGCTGCTGCCGCCC	GRCh37
NC_000006.10:g.139736238_139736265delinsAGAGCCGCCGGGGGTGCTGCTGCCGCCC	NCBI36
NG_016169.1:g.6214_6241delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT MANE Select	ENSP00000356623.2:p.Ser170=
ENST00000367651.3:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	ENSP00000356623.2:p.Ser170=
ENST00000536159.2:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	ENSP00000442831.1:p.Ser170=
ENST00000537332.2:c.525_552delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	ENSP00000444198.2:p.Ser175=
ENST00000618718.1:c.476+34_476+61delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	ENSP00000479918.1:n.476+34_476+61delinsGGGCGGCAGCAGCACCCCCGGC...
NM_001168388.2:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	NP_001161860.1:p.Ser170=
NM_001168389.2:c.525_552delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	NP_001161861.2:p.Ser175=
NM_006079.4:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	NP_006070.2:p.Ser170=
NM_006079.5:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT MANE Select	NP_006070.2:p.Ser170=
NM_001168388.3:c.510_537delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	NP_001161860.1:p.Ser170=
NM_001168389.3:c.525_552delinsGGGCGGCAGCAGCACCCCCGGCGGCTCT	NP_001161861.2:p.Ser175=