Canonical Allele Identifier: CA2773276764
Gene: CITED2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373400_139373403del , CM000668.2:g.139373400_139373403del GRCh38
NC_000006.11:g.139694537_139694540del , CM000668.1:g.139694537_139694540del GRCh37
NC_000006.10:g.139736230_139736233del NCBI36
NG_016169.1:g.6246_6249del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.542_545del MANE Select ENSP00000356623.2:p.Ser181ThrfsTer?
ENST00000367651.3:c.542_545del ENSP00000356623.2:p.Ser181ThrfsTer?
ENST00000536159.2:c.542_545del ENSP00000442831.1:p.Ser181ThrfsTer?
ENST00000537332.2:c.557_560del ENSP00000444198.2:p.Ser186ThrfsTer?
ENST00000618718.1:c.476+66_476+69del ENSP00000479918.1:n.476+66_476+69del
NM_001168388.2:c.542_545del NP_001161860.1:p.Ser181ThrfsTer?
NM_001168389.2:c.557_560del NP_001161861.2:p.Ser186ThrfsTer?
NM_006079.4:c.542_545del NP_006070.2:p.Ser181ThrfsTer?
NM_006079.5:c.542_545del MANE Select NP_006070.2:p.Ser181ThrfsTer?
NM_001168388.3:c.542_545del NP_001161860.1:p.Ser181ThrfsTer?
NM_001168389.3:c.557_560del NP_001161861.2:p.Ser186ThrfsTer?