Canonical Allele Identifier: CA1667372003

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372785_139372786delinsCA , CM000668.2:g.139372785_139372786delinsCA	GRCh38
NC_000006.11:g.139693922_139693923delinsCA , CM000668.1:g.139693922_139693923delinsCA	GRCh37
NC_000006.10:g.139735615_139735616delinsCA	NCBI36
NG_016169.1:g.6863_6864delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*346_*347delinsTG MANE Select	ENSP00000356623.2:n.*346_*347delinsTG
ENST00000367651.3:c.*346_*347delinsTG	ENSP00000356623.2:n.*346_*347delinsTG
ENST00000536159.2:c.*346_*347delinsTG	ENSP00000442831.1:n.*346_*347delinsTG
ENST00000537332.2:c.*346_*347delinsTG	ENSP00000444198.2:n.*346_*347delinsTG
NM_001168388.2:c.*346_*347delinsTG	NP_001161860.1:n.*346_*347delinsTG
NM_001168389.2:c.*346_*347delinsTG	NP_001161861.2:n.*346_*347delinsTG
NM_006079.4:c.*346_*347delinsTG	NP_006070.2:n.*346_*347delinsTG
NM_006079.5:c.*346_*347delinsTG MANE Select	NP_006070.2:n.*346_*347delinsTG
NM_001168388.3:c.*346_*347delinsTG	NP_001161860.1:n.*346_*347delinsTG
NM_001168389.3:c.*346_*347delinsTG	NP_001161861.2:n.*346_*347delinsTG