Canonical Allele Identifier: CA917872448

Gene: CITED2

Linked Data

• dbSNP Id: rs1562313891

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372915_139372919dup , CM000668.2:g.139372915_139372919dup	GRCh38
NC_000006.11:g.139694052_139694056dup , CM000668.1:g.139694052_139694056dup	GRCh37
NC_000006.10:g.139735745_139735749dup	NCBI36
NG_016169.1:g.6730_6734dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*213_*217dup MANE Select	ENSP00000356623.2:n.*213_*217dup
ENST00000367651.3:c.*213_*217dup	ENSP00000356623.2:n.*213_*217dup
ENST00000536159.2:c.*213_*217dup	ENSP00000442831.1:n.*213_*217dup
ENST00000537332.2:c.*213_*217dup	ENSP00000444198.2:n.*213_*217dup
NM_001168388.2:c.*213_*217dup	NP_001161860.1:n.*213_*217dup
NM_001168389.2:c.*213_*217dup	NP_001161861.2:n.*213_*217dup
NM_006079.4:c.*213_*217dup	NP_006070.2:n.*213_*217dup
NM_006079.5:c.*213_*217dup MANE Select	NP_006070.2:n.*213_*217dup
NM_001168388.3:c.*213_*217dup	NP_001161860.1:n.*213_*217dup
NM_001168389.3:c.*213_*217dup	NP_001161861.2:n.*213_*217dup