Canonical Allele Identifier: CA1667371973

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372727_139372728delinsTC , CM000668.2:g.139372727_139372728delinsTC	GRCh38
NC_000006.11:g.139693864_139693865delinsTC , CM000668.1:g.139693864_139693865delinsTC	GRCh37
NC_000006.10:g.139735557_139735558delinsTC	NCBI36
NG_016169.1:g.6921_6922delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*404_*405delinsGA MANE Select	ENSP00000356623.2:n.*404_*405delinsGA
ENST00000367651.3:c.*404_*405delinsGA	ENSP00000356623.2:n.*404_*405delinsGA
ENST00000536159.2:c.*404_*405delinsGA	ENSP00000442831.1:n.*404_*405delinsGA
ENST00000537332.2:c.*404_*405delinsGA	ENSP00000444198.2:n.*404_*405delinsGA
NM_001168388.2:c.*404_*405delinsGA	NP_001161860.1:n.*404_*405delinsGA
NM_001168389.2:c.*404_*405delinsGA	NP_001161861.2:n.*404_*405delinsGA
NM_006079.4:c.*404_*405delinsGA	NP_006070.2:n.*404_*405delinsGA
NM_006079.5:c.*404_*405delinsGA MANE Select	NP_006070.2:n.*404_*405delinsGA
NM_001168388.3:c.*404_*405delinsGA	NP_001161860.1:n.*404_*405delinsGA
NM_001168389.3:c.*404_*405delinsGA	NP_001161861.2:n.*404_*405delinsGA