Canonical Allele Identifier: CA1667372156

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373005C= , CM000668.2:g.139373005C=	GRCh38
NC_000006.11:g.139694142C= , CM000668.1:g.139694142C=	GRCh37
NC_000006.10:g.139735835C=	NCBI36
NG_016169.1:g.6644G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*127G= MANE Select	ENSP00000356623.2:n.*127G=
ENST00000367651.3:c.*127G=	ENSP00000356623.2:n.*127G=
ENST00000536159.2:c.*127G=	ENSP00000442831.1:n.*127G=
ENST00000537332.2:c.*127G=	ENSP00000444198.2:n.*127G=
NM_001168388.2:c.*127G=	NP_001161860.1:n.*127G=
NM_001168389.2:c.*127G=	NP_001161861.2:n.*127G=
NM_006079.4:c.*127G=	NP_006070.2:n.*127G=
NM_006079.5:c.*127G= MANE Select	NP_006070.2:n.*127G=
NM_001168388.3:c.*127G=	NP_001161860.1:n.*127G=
NM_001168389.3:c.*127G=	NP_001161861.2:n.*127G=