Canonical Allele Identifier: CA1667372275

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373241_139373243delinsATT , CM000668.2:g.139373241_139373243delinsATT	GRCh38
NC_000006.11:g.139694378_139694380delinsATT , CM000668.1:g.139694378_139694380delinsATT	GRCh37
NC_000006.10:g.139736071_139736073delinsATT	NCBI36
NG_016169.1:g.6406_6408delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.702_704delinsAAT MANE Select	ENSP00000356623.2:p.Glu234=
ENST00000367651.3:c.702_704delinsAAT	ENSP00000356623.2:p.Glu234=
ENST00000536159.2:c.702_704delinsAAT	ENSP00000442831.1:p.Glu234=
ENST00000537332.2:c.717_719delinsAAT	ENSP00000444198.2:p.Glu239=
ENST00000618718.1:c.531_533delinsAAT	ENSP00000479918.1:p.Glu177=
NM_001168388.2:c.702_704delinsAAT	NP_001161860.1:p.Glu234=
NM_001168389.2:c.717_719delinsAAT	NP_001161861.2:p.Glu239=
NM_006079.4:c.702_704delinsAAT	NP_006070.2:p.Glu234=
NM_006079.5:c.702_704delinsAAT MANE Select	NP_006070.2:p.Glu234=
NM_001168388.3:c.702_704delinsAAT	NP_001161860.1:p.Glu234=
NM_001168389.3:c.717_719delinsAAT	NP_001161861.2:p.Glu239=