Canonical Allele Identifier: CA1667372254

Gene: CITED2

Linked Data

• dbSNP Id: rs1778287251

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373167_139373168del , CM000668.2:g.139373167_139373168del	GRCh38
NC_000006.11:g.139694304_139694305del , CM000668.1:g.139694304_139694305del	GRCh37
NC_000006.10:g.139735997_139735998del	NCBI36
NG_016169.1:g.6481_6482del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367651.4:c.777_778del MANE Select	ENSP00000356623.2:p.Cys261GlnfsTer?
ENST00000367651.3:c.777_778del	ENSP00000356623.2:p.Cys261GlnfsTer?
ENST00000536159.2:c.777_778del	ENSP00000442831.1:p.Cys261GlnfsTer?
ENST00000537332.2:c.792_793del	ENSP00000444198.2:p.Cys266GlnfsTer?
ENST00000618718.1:c.606_607del	ENSP00000479918.1:p.Cys204GlnfsTer?
NM_001168388.2:c.777_778del	NP_001161860.1:p.Cys261GlnfsTer?
NM_001168389.2:c.792_793del	NP_001161861.2:p.Cys266GlnfsTer?
NM_006079.4:c.777_778del	NP_006070.2:p.Cys261GlnfsTer?
NM_006079.5:c.777_778del MANE Select	NP_006070.2:p.Cys261GlnfsTer?
NM_001168388.3:c.777_778del	NP_001161860.1:p.Cys261GlnfsTer?
NM_001168389.3:c.792_793del	NP_001161861.2:p.Cys266GlnfsTer?