Canonical Allele Identifier: CA4025577
Gene: CITED2 HGNC NCBI

Linked Data

dbSNP Id: rs756787827

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.139373370_139373372del , CM000668.2:g.139373370_139373372del GRCh38
NC_000006.11:g.139694507_139694509del , CM000668.1:g.139694507_139694509del GRCh37
NC_000006.10:g.139736200_139736202del NCBI36
NG_016169.1:g.6278_6280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367651.4:c.574_576del MANE Select ENSP00000356623.2:p.Ser192del
ENST00000367651.3:c.574_576del ENSP00000356623.2:p.Ser192del
ENST00000536159.2:c.574_576del ENSP00000442831.1:p.Ser192del
ENST00000537332.2:c.589_591del ENSP00000444198.2:p.Ser197del
ENST00000618718.1:c.477-74_477-72del ENSP00000479918.1:n.477-74_477-72del
NM_001168388.2:c.574_576del NP_001161860.1:p.Ser192del
NM_001168389.2:c.589_591del NP_001161861.2:p.Ser197del
NM_006079.4:c.574_576del NP_006070.2:p.Ser192del
NM_006079.5:c.574_576del MANE Select NP_006070.2:p.Ser192del
NM_001168388.3:c.574_576del NP_001161860.1:p.Ser192del
NM_001168389.3:c.589_591del NP_001161861.2:p.Ser197del