Canonical Allele Identifier: CA2680562312

Gene: CITED2

Linked Data

• gnomAD v4: 6-139372823-TGAGCACTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372827_139372834del , CM000668.2:g.139372827_139372834del	GRCh38
NC_000006.11:g.139693964_139693971del , CM000668.1:g.139693964_139693971del	GRCh37
NC_000006.10:g.139735657_139735664del	NCBI36
NG_016169.1:g.6818_6825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*301_*308del MANE Select	ENSP00000356623.2:n.*301_*308del
ENST00000367651.3:c.*301_*308del	ENSP00000356623.2:n.*301_*308del
ENST00000536159.2:c.*301_*308del	ENSP00000442831.1:n.*301_*308del
ENST00000537332.2:c.*301_*308del	ENSP00000444198.2:n.*301_*308del
NM_001168388.2:c.*301_*308del	NP_001161860.1:n.*301_*308del
NM_001168389.2:c.*301_*308del	NP_001161861.2:n.*301_*308del
NM_006079.4:c.*301_*308del	NP_006070.2:n.*301_*308del
NM_006079.5:c.*301_*308del MANE Select	NP_006070.2:n.*301_*308del
NM_001168388.3:c.*301_*308del	NP_001161860.1:n.*301_*308del
NM_001168389.3:c.*301_*308del	NP_001161861.2:n.*301_*308del