Canonical Allele Identifier: CA2680562338
Gene: CITED2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139372854_139372857del , CM000668.2:g.139372854_139372857del GRCh38
NC_000006.11:g.139693991_139693994del , CM000668.1:g.139693991_139693994del GRCh37
NC_000006.10:g.139735684_139735687del NCBI36
NG_016169.1:g.6793_6796del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.*276_*279del MANE Select ENSP00000356623.2:n.*276_*279del
ENST00000367651.3:c.*276_*279del ENSP00000356623.2:n.*276_*279del
ENST00000536159.2:c.*276_*279del ENSP00000442831.1:n.*276_*279del
ENST00000537332.2:c.*276_*279del ENSP00000444198.2:n.*276_*279del
NM_001168388.2:c.*276_*279del NP_001161860.1:n.*276_*279del
NM_001168389.2:c.*276_*279del NP_001161861.2:n.*276_*279del
NM_006079.4:c.*276_*279del NP_006070.2:n.*276_*279del
NM_006079.5:c.*276_*279del MANE Select NP_006070.2:n.*276_*279del
NM_001168388.3:c.*276_*279del NP_001161860.1:n.*276_*279del
NM_001168389.3:c.*276_*279del NP_001161861.2:n.*276_*279del