Canonical Allele Identifier: CA1667372192
Gene: CITED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373069_139373072delinsTTTC , CM000668.2:g.139373069_139373072delinsTTTC GRCh38
NC_000006.11:g.139694206_139694209delinsTTTC , CM000668.1:g.139694206_139694209delinsTTTC GRCh37
NC_000006.10:g.139735899_139735902delinsTTTC NCBI36
NG_016169.1:g.6577_6580delinsGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*60_*63delinsGAAA MANE Select ENSP00000356623.2:n.*60_*63delinsGAAA
ENST00000367651.3:c.*60_*63delinsGAAA ENSP00000356623.2:n.*60_*63delinsGAAA
ENST00000536159.2:c.*60_*63delinsGAAA ENSP00000442831.1:n.*60_*63delinsGAAA
ENST00000537332.2:c.*60_*63delinsGAAA ENSP00000444198.2:n.*60_*63delinsGAAA
NM_001168388.2:c.*60_*63delinsGAAA NP_001161860.1:n.*60_*63delinsGAAA
NM_001168389.2:c.*60_*63delinsGAAA NP_001161861.2:n.*60_*63delinsGAAA
NM_006079.4:c.*60_*63delinsGAAA NP_006070.2:n.*60_*63delinsGAAA
NM_006079.5:c.*60_*63delinsGAAA MANE Select NP_006070.2:n.*60_*63delinsGAAA
NM_001168388.3:c.*60_*63delinsGAAA NP_001161860.1:n.*60_*63delinsGAAA
NM_001168389.3:c.*60_*63delinsGAAA NP_001161861.2:n.*60_*63delinsGAAA