Canonical Allele Identifier: CA1667372164

Gene: CITED2

Linked Data

• dbSNP Id: rs1778282832

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373016_139373017insCTTA , CM000668.2:g.139373016_139373017insCTTA	GRCh38
NC_000006.11:g.139694153_139694154insCTTA , CM000668.1:g.139694153_139694154insCTTA	GRCh37
NC_000006.10:g.139735846_139735847insCTTA	NCBI36
NG_016169.1:g.6633_6634insAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*116_*117insAAGT MANE Select	ENSP00000356623.2:n.*116_*117insAAGT
ENST00000367651.3:c.*116_*117insAAGT	ENSP00000356623.2:n.*116_*117insAAGT
ENST00000536159.2:c.*116_*117insAAGT	ENSP00000442831.1:n.*116_*117insAAGT
ENST00000537332.2:c.*116_*117insAAGT	ENSP00000444198.2:n.*116_*117insAAGT
NM_001168388.2:c.*116_*117insAAGT	NP_001161860.1:n.*116_*117insAAGT
NM_001168389.2:c.*116_*117insAAGT	NP_001161861.2:n.*116_*117insAAGT
NM_006079.4:c.*116_*117insAAGT	NP_006070.2:n.*116_*117insAAGT
NM_006079.5:c.*116_*117insAAGT MANE Select	NP_006070.2:n.*116_*117insAAGT
NM_001168388.3:c.*116_*117insAAGT	NP_001161860.1:n.*116_*117insAAGT
NM_001168389.3:c.*116_*117insAAGT	NP_001161861.2:n.*116_*117insAAGT