Canonical Allele Identifier: CA1667372302

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373315_139373316delinsAG , CM000668.2:g.139373315_139373316delinsAG	GRCh38
NC_000006.11:g.139694452_139694453delinsAG , CM000668.1:g.139694452_139694453delinsAG	GRCh37
NC_000006.10:g.139736145_139736146delinsAG	NCBI36
NG_016169.1:g.6333_6334delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.629_630delinsCT MANE Select	ENSP00000356623.2:p.Ala210=
ENST00000367651.3:c.629_630delinsCT	ENSP00000356623.2:p.Ala210=
ENST00000536159.2:c.629_630delinsCT	ENSP00000442831.1:p.Ala210=
ENST00000537332.2:c.644_645delinsCT	ENSP00000444198.2:p.Ala215=
ENST00000618718.1:c.477-19_477-18delinsCT	ENSP00000479918.1:n.477-19_477-18delinsCT
NM_001168388.2:c.629_630delinsCT	NP_001161860.1:p.Ala210=
NM_001168389.2:c.644_645delinsCT	NP_001161861.2:p.Ala215=
NM_006079.4:c.629_630delinsCT	NP_006070.2:p.Ala210=
NM_006079.5:c.629_630delinsCT MANE Select	NP_006070.2:p.Ala210=
NM_001168388.3:c.629_630delinsCT	NP_001161860.1:p.Ala210=
NM_001168389.3:c.644_645delinsCT	NP_001161861.2:p.Ala215=