Canonical Allele Identifier: CA1667372058
Gene: CITED2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372860_139372862delinsAAC , CM000668.2:g.139372860_139372862delinsAAC GRCh38
NC_000006.11:g.139693997_139693999delinsAAC , CM000668.1:g.139693997_139693999delinsAAC GRCh37
NC_000006.10:g.139735690_139735692delinsAAC NCBI36
NG_016169.1:g.6787_6789delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*270_*272delinsGTT MANE Select ENSP00000356623.2:n.*270_*272delinsGTT
ENST00000367651.3:c.*270_*272delinsGTT ENSP00000356623.2:n.*270_*272delinsGTT
ENST00000536159.2:c.*270_*272delinsGTT ENSP00000442831.1:n.*270_*272delinsGTT
ENST00000537332.2:c.*270_*272delinsGTT ENSP00000444198.2:n.*270_*272delinsGTT
NM_001168388.2:c.*270_*272delinsGTT NP_001161860.1:n.*270_*272delinsGTT
NM_001168389.2:c.*270_*272delinsGTT NP_001161861.2:n.*270_*272delinsGTT
NM_006079.4:c.*270_*272delinsGTT NP_006070.2:n.*270_*272delinsGTT
NM_006079.5:c.*270_*272delinsGTT MANE Select NP_006070.2:n.*270_*272delinsGTT
NM_001168388.3:c.*270_*272delinsGTT NP_001161860.1:n.*270_*272delinsGTT
NM_001168389.3:c.*270_*272delinsGTT NP_001161861.2:n.*270_*272delinsGTT
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