Canonical Allele Identifier: CA2713330466

Gene: CITED2

Linked Data

• dbSNP Id: rs2114777182

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373356_139373376del , CM000668.2:g.139373356_139373376del	GRCh38
NC_000006.11:g.139694493_139694513del , CM000668.1:g.139694493_139694513del	GRCh37
NC_000006.10:g.139736186_139736206del	NCBI36
NG_016169.1:g.6276_6296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.572_592del MANE Select	ENSP00000356623.2:p.Asn191_Gly197del
ENST00000367651.3:c.572_592del	ENSP00000356623.2:p.Asn191_Gly197del
ENST00000536159.2:c.572_592del	ENSP00000442831.1:p.Asn191_Gly197del
ENST00000537332.2:c.587_607del	ENSP00000444198.2:p.Asn196_Gly202del
ENST00000618718.1:c.477-76_477-56del	ENSP00000479918.1:n.477-76_477-56del
NM_001168388.2:c.572_592del	NP_001161860.1:p.Asn191_Gly197del
NM_001168389.2:c.587_607del	NP_001161861.2:p.Asn196_Gly202del
NM_006079.4:c.572_592del	NP_006070.2:p.Asn191_Gly197del
NM_006079.5:c.572_592del MANE Select	NP_006070.2:p.Asn191_Gly197del
NM_001168388.3:c.572_592del	NP_001161860.1:p.Asn191_Gly197del
NM_001168389.3:c.587_607del	NP_001161861.2:p.Asn196_Gly202del