Canonical Allele Identifier: CA1667372214

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373096G= , CM000668.2:g.139373096G=	GRCh38
NC_000006.11:g.139694233G= , CM000668.1:g.139694233G=	GRCh37
NC_000006.10:g.139735926G=	NCBI36
NG_016169.1:g.6553C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.*36C= MANE Select	ENSP00000356623.2:n.*36C=
ENST00000367651.3:c.*36C=	ENSP00000356623.2:n.*36C=
ENST00000536159.2:c.*36C=	ENSP00000442831.1:n.*36C=
ENST00000537332.2:c.*36C=	ENSP00000444198.2:n.*36C=
ENST00000618718.1:c.*36C=	ENSP00000479918.1:n.*36C=
NM_001168388.2:c.*36C=	NP_001161860.1:n.*36C=
NM_001168389.2:c.*36C=	NP_001161861.2:n.*36C=
NM_006079.4:c.*36C=	NP_006070.2:n.*36C=
NM_006079.5:c.*36C= MANE Select	NP_006070.2:n.*36C=
NM_001168388.3:c.*36C=	NP_001161860.1:n.*36C=
NM_001168389.3:c.*36C=	NP_001161861.2:n.*36C=