Canonical Allele Identifier: CA1667372253

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373166_139373168delinsACG , CM000668.2:g.139373166_139373168delinsACG	GRCh38
NC_000006.11:g.139694303_139694305delinsACG , CM000668.1:g.139694303_139694305delinsACG	GRCh37
NC_000006.10:g.139735996_139735998delinsACG	NCBI36
NG_016169.1:g.6481_6483delinsCGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367651.4:c.777_779delinsCGT MANE Select	ENSP00000356623.2:p.Phe259=
ENST00000367651.3:c.777_779delinsCGT	ENSP00000356623.2:p.Phe259=
ENST00000536159.2:c.777_779delinsCGT	ENSP00000442831.1:p.Phe259=
ENST00000537332.2:c.792_794delinsCGT	ENSP00000444198.2:p.Phe264=
ENST00000618718.1:c.606_608delinsCGT	ENSP00000479918.1:p.Phe202=
NM_001168388.2:c.777_779delinsCGT	NP_001161860.1:p.Phe259=
NM_001168389.2:c.792_794delinsCGT	NP_001161861.2:p.Phe264=
NM_006079.4:c.777_779delinsCGT	NP_006070.2:p.Phe259=
NM_006079.5:c.777_779delinsCGT MANE Select	NP_006070.2:p.Phe259=
NM_001168388.3:c.777_779delinsCGT	NP_001161860.1:p.Phe259=
NM_001168389.3:c.792_794delinsCGT	NP_001161861.2:p.Phe264=