Canonical Allele Identifier: CA1667372005

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139372791T= , CM000668.2:g.139372791T=	GRCh38
NC_000006.11:g.139693928T= , CM000668.1:g.139693928T=	GRCh37
NC_000006.10:g.139735621T=	NCBI36
NG_016169.1:g.6858A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*341A= MANE Select	ENSP00000356623.2:n.*341A=
ENST00000367651.3:c.*341A=	ENSP00000356623.2:n.*341A=
ENST00000536159.2:c.*341A=	ENSP00000442831.1:n.*341A=
ENST00000537332.2:c.*341A=	ENSP00000444198.2:n.*341A=
NM_001168388.2:c.*341A=	NP_001161860.1:n.*341A=
NM_001168389.2:c.*341A=	NP_001161861.2:n.*341A=
NM_006079.4:c.*341A=	NP_006070.2:n.*341A=
NM_006079.5:c.*341A= MANE Select	NP_006070.2:n.*341A=
NM_001168388.3:c.*341A=	NP_001161860.1:n.*341A=
NM_001168389.3:c.*341A=	NP_001161861.2:n.*341A=