Canonical Allele Identifier: CA1667372379

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373399G= , CM000668.2:g.139373399G=	GRCh38
NC_000006.11:g.139694536G= , CM000668.1:g.139694536G=	GRCh37
NC_000006.10:g.139736229G=	NCBI36
NG_016169.1:g.6250C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.546C= MANE Select	ENSP00000356623.2:p.Ser182=
ENST00000367651.3:c.546C=	ENSP00000356623.2:p.Ser182=
ENST00000536159.2:c.546C=	ENSP00000442831.1:p.Ser182=
ENST00000537332.2:c.561C=	ENSP00000444198.2:p.Ser187=
ENST00000618718.1:c.476+70C=	ENSP00000479918.1:n.476+70C=
NM_001168388.2:c.546C=	NP_001161860.1:p.Ser182=
NM_001168389.2:c.561C=	NP_001161861.2:p.Ser187=
NM_006079.4:c.546C=	NP_006070.2:p.Ser182=
NM_006079.5:c.546C= MANE Select	NP_006070.2:p.Ser182=
NM_001168388.3:c.546C=	NP_001161860.1:p.Ser182=
NM_001168389.3:c.561C=	NP_001161861.2:p.Ser187=