Canonical Allele Identifier: CA1667372114

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372946_139372948delinsCAG , CM000668.2:g.139372946_139372948delinsCAG	GRCh38
NC_000006.11:g.139694083_139694085delinsCAG , CM000668.1:g.139694083_139694085delinsCAG	GRCh37
NC_000006.10:g.139735776_139735778delinsCAG	NCBI36
NG_016169.1:g.6701_6703delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*184_*186delinsCTG MANE Select	ENSP00000356623.2:n.*184_*186delinsCTG
ENST00000367651.3:c.*184_*186delinsCTG	ENSP00000356623.2:n.*184_*186delinsCTG
ENST00000536159.2:c.*184_*186delinsCTG	ENSP00000442831.1:n.*184_*186delinsCTG
ENST00000537332.2:c.*184_*186delinsCTG	ENSP00000444198.2:n.*184_*186delinsCTG
NM_001168388.2:c.*184_*186delinsCTG	NP_001161860.1:n.*184_*186delinsCTG
NM_001168389.2:c.*184_*186delinsCTG	NP_001161861.2:n.*184_*186delinsCTG
NM_006079.4:c.*184_*186delinsCTG	NP_006070.2:n.*184_*186delinsCTG
NM_006079.5:c.*184_*186delinsCTG MANE Select	NP_006070.2:n.*184_*186delinsCTG
NM_001168388.3:c.*184_*186delinsCTG	NP_001161860.1:n.*184_*186delinsCTG
NM_001168389.3:c.*184_*186delinsCTG	NP_001161861.2:n.*184_*186delinsCTG