Canonical Allele Identifier: CA1667371962

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372711_139372715delinsCAACT , CM000668.2:g.139372711_139372715delinsCAACT	GRCh38
NC_000006.11:g.139693848_139693852delinsCAACT , CM000668.1:g.139693848_139693852delinsCAACT	GRCh37
NC_000006.10:g.139735541_139735545delinsCAACT	NCBI36
NG_016169.1:g.6934_6938delinsAGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*417_*421delinsAGTTG MANE Select	ENSP00000356623.2:n.*417_*421delinsAGTTG
ENST00000367651.3:c.*417_*421delinsAGTTG	ENSP00000356623.2:n.*417_*421delinsAGTTG
ENST00000536159.2:c.*417_*421delinsAGTTG	ENSP00000442831.1:n.*417_*421delinsAGTTG
ENST00000537332.2:c.*417_*421delinsAGTTG	ENSP00000444198.2:n.*417_*421delinsAGTTG
NM_001168388.2:c.*417_*421delinsAGTTG	NP_001161860.1:n.*417_*421delinsAGTTG
NM_001168389.2:c.*417_*421delinsAGTTG	NP_001161861.2:n.*417_*421delinsAGTTG
NM_006079.4:c.*417_*421delinsAGTTG	NP_006070.2:n.*417_*421delinsAGTTG
NM_006079.5:c.*417_*421delinsAGTTG MANE Select	NP_006070.2:n.*417_*421delinsAGTTG
NM_001168388.3:c.*417_*421delinsAGTTG	NP_001161860.1:n.*417_*421delinsAGTTG
NM_001168389.3:c.*417_*421delinsAGTTG	NP_001161861.2:n.*417_*421delinsAGTTG