Canonical Allele Identifier: CA1667372351

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373366G= , CM000668.2:g.139373366G=	GRCh38
NC_000006.11:g.139694503G= , CM000668.1:g.139694503G=	GRCh37
NC_000006.10:g.139736196G=	NCBI36
NG_016169.1:g.6283C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.579C= MANE Select	ENSP00000356623.2:p.Gly193=
ENST00000367651.3:c.579C=	ENSP00000356623.2:p.Gly193=
ENST00000536159.2:c.579C=	ENSP00000442831.1:p.Gly193=
ENST00000537332.2:c.594C=	ENSP00000444198.2:p.Gly198=
ENST00000618718.1:c.477-69C=	ENSP00000479918.1:n.477-69C=
NM_001168388.2:c.579C=	NP_001161860.1:p.Gly193=
NM_001168389.2:c.594C=	NP_001161861.2:p.Gly198=
NM_006079.4:c.579C=	NP_006070.2:p.Gly193=
NM_006079.5:c.579C= MANE Select	NP_006070.2:p.Gly193=
NM_001168388.3:c.579C=	NP_001161860.1:p.Gly193=
NM_001168389.3:c.594C=	NP_001161861.2:p.Gly198=