Canonical Allele Identifier: CA2680562347

Gene: CITED2

Linked Data

• gnomAD v4: 6-139372862-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372864del , CM000668.2:g.139372864del	GRCh38
NC_000006.11:g.139694001del , CM000668.1:g.139694001del	GRCh37
NC_000006.10:g.139735694del	NCBI36
NG_016169.1:g.6786del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*269del MANE Select	ENSP00000356623.2:n.*269del
ENST00000367651.3:c.*269del	ENSP00000356623.2:n.*269del
ENST00000536159.2:c.*269del	ENSP00000442831.1:n.*269del
ENST00000537332.2:c.*269del	ENSP00000444198.2:n.*269del
NM_001168388.2:c.*269del	NP_001161860.1:n.*269del
NM_001168389.2:c.*269del	NP_001161861.2:n.*269del
NM_006079.4:c.*269del	NP_006070.2:n.*269del
NM_006079.5:c.*269del MANE Select	NP_006070.2:n.*269del
NM_001168388.3:c.*269del	NP_001161860.1:n.*269del
NM_001168389.3:c.*269del	NP_001161861.2:n.*269del