Canonical Allele Identifier: CA1667372296

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373298T= , CM000668.2:g.139373298T=	GRCh38
NC_000006.11:g.139694435T= , CM000668.1:g.139694435T=	GRCh37
NC_000006.10:g.139736128T=	NCBI36
NG_016169.1:g.6351A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.647A= MANE Select	ENSP00000356623.2:p.Asn216=
ENST00000367651.3:c.647A=	ENSP00000356623.2:p.Asn216=
ENST00000536159.2:c.647A=	ENSP00000442831.1:p.Asn216=
ENST00000537332.2:c.662A=	ENSP00000444198.2:p.Asn221=
ENST00000618718.1:c.477-1A=	ENSP00000479918.1:n.477-1A=
NM_001168388.2:c.647A=	NP_001161860.1:p.Asn216=
NM_001168389.2:c.662A=	NP_001161861.2:p.Asn221=
NM_006079.4:c.647A=	NP_006070.2:p.Asn216=
NM_006079.5:c.647A= MANE Select	NP_006070.2:p.Asn216=
NM_001168388.3:c.647A=	NP_001161860.1:p.Asn216=
NM_001168389.3:c.662A=	NP_001161861.2:p.Asn221=