Canonical Allele Identifier: CA1667371978

Gene: CITED2

Linked Data

• dbSNP Id: rs1778273030
• gnomAD v4: 6-139372731-TTCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372734_139372737del , CM000668.2:g.139372734_139372737del	GRCh38
NC_000006.11:g.139693871_139693874del , CM000668.1:g.139693871_139693874del	GRCh37
NC_000006.10:g.139735564_139735567del	NCBI36
NG_016169.1:g.6914_6917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*397_*400del MANE Select	ENSP00000356623.2:n.*397_*400del
ENST00000367651.3:c.*397_*400del	ENSP00000356623.2:n.*397_*400del
ENST00000536159.2:c.*397_*400del	ENSP00000442831.1:n.*397_*400del
ENST00000537332.2:c.*397_*400del	ENSP00000444198.2:n.*397_*400del
NM_001168388.2:c.*397_*400del	NP_001161860.1:n.*397_*400del
NM_001168389.2:c.*397_*400del	NP_001161861.2:n.*397_*400del
NM_006079.4:c.*397_*400del	NP_006070.2:n.*397_*400del
NM_006079.5:c.*397_*400del MANE Select	NP_006070.2:n.*397_*400del
NM_001168388.3:c.*397_*400del	NP_001161860.1:n.*397_*400del
NM_001168389.3:c.*397_*400del	NP_001161861.2:n.*397_*400del