Canonical Allele Identifier: CA4025581
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs780870084

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373384_139373407del , CM000668.2:g.139373384_139373407del GRCh38
NC_000006.11:g.139694521_139694544del , CM000668.1:g.139694521_139694544del GRCh37
NC_000006.10:g.139736214_139736237del NCBI36
NG_016169.1:g.6251_6274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.547_570del MANE Select ENSP00000356623.2:p.Ser183_Ser190del
ENST00000367651.3:c.547_570del ENSP00000356623.2:p.Ser183_Ser190del
ENST00000536159.2:c.547_570del ENSP00000442831.1:p.Ser183_Ser190del
ENST00000537332.2:c.562_585del ENSP00000444198.2:p.Ser188_Ser195del
ENST00000618718.1:c.476+71_477-78del ENSP00000479918.1:n.476+71_477-78del
NM_001168388.2:c.547_570del NP_001161860.1:p.Ser183_Ser190del
NM_001168389.2:c.562_585del NP_001161861.2:p.Ser188_Ser195del
NM_006079.4:c.547_570del NP_006070.2:p.Ser183_Ser190del
NM_006079.5:c.547_570del MANE Select NP_006070.2:p.Ser183_Ser190del
NM_001168388.3:c.547_570del NP_001161860.1:p.Ser183_Ser190del
NM_001168389.3:c.562_585del NP_001161861.2:p.Ser188_Ser195del