Canonical Allele Identifier: CA1667371977

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372731_139372735delinsTTCAC , CM000668.2:g.139372731_139372735delinsTTCAC	GRCh38
NC_000006.11:g.139693868_139693872delinsTTCAC , CM000668.1:g.139693868_139693872delinsTTCAC	GRCh37
NC_000006.10:g.139735561_139735565delinsTTCAC	NCBI36
NG_016169.1:g.6914_6918delinsGTGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*397_*401delinsGTGAA MANE Select	ENSP00000356623.2:n.*397_*401delinsGTGAA
ENST00000367651.3:c.*397_*401delinsGTGAA	ENSP00000356623.2:n.*397_*401delinsGTGAA
ENST00000536159.2:c.*397_*401delinsGTGAA	ENSP00000442831.1:n.*397_*401delinsGTGAA
ENST00000537332.2:c.*397_*401delinsGTGAA	ENSP00000444198.2:n.*397_*401delinsGTGAA
NM_001168388.2:c.*397_*401delinsGTGAA	NP_001161860.1:n.*397_*401delinsGTGAA
NM_001168389.2:c.*397_*401delinsGTGAA	NP_001161861.2:n.*397_*401delinsGTGAA
NM_006079.4:c.*397_*401delinsGTGAA	NP_006070.2:n.*397_*401delinsGTGAA
NM_006079.5:c.*397_*401delinsGTGAA MANE Select	NP_006070.2:n.*397_*401delinsGTGAA
NM_001168388.3:c.*397_*401delinsGTGAA	NP_001161860.1:n.*397_*401delinsGTGAA
NM_001168389.3:c.*397_*401delinsGTGAA	NP_001161861.2:n.*397_*401delinsGTGAA