Canonical Allele Identifier: CA1667372256

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373169A= , CM000668.2:g.139373169A=	GRCh38
NC_000006.11:g.139694306A= , CM000668.1:g.139694306A=	GRCh37
NC_000006.10:g.139735999A=	NCBI36
NG_016169.1:g.6480T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.776T= MANE Select	ENSP00000356623.2:p.Phe259=
ENST00000367651.3:c.776T=	ENSP00000356623.2:p.Phe259=
ENST00000536159.2:c.776T=	ENSP00000442831.1:p.Phe259=
ENST00000537332.2:c.791T=	ENSP00000444198.2:p.Phe264=
ENST00000618718.1:c.605T=	ENSP00000479918.1:p.Phe202=
NM_001168388.2:c.776T=	NP_001161860.1:p.Phe259=
NM_001168389.2:c.791T=	NP_001161861.2:p.Phe264=
NM_006079.4:c.776T=	NP_006070.2:p.Phe259=
NM_006079.5:c.776T= MANE Select	NP_006070.2:p.Phe259=
NM_001168388.3:c.776T=	NP_001161860.1:p.Phe259=
NM_001168389.3:c.791T=	NP_001161861.2:p.Phe264=