Canonical Allele Identifier: CA2773276763

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373398dup , CM000668.2:g.139373398dup	GRCh38
NC_000006.11:g.139694535dup , CM000668.1:g.139694535dup	GRCh37
NC_000006.10:g.139736228dup	NCBI36
NG_016169.1:g.6251dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.547dup MANE Select	ENSP00000356623.2:p.Ser183PhefsTer?
ENST00000367651.3:c.547dup	ENSP00000356623.2:p.Ser183PhefsTer?
ENST00000536159.2:c.547dup	ENSP00000442831.1:p.Ser183PhefsTer?
ENST00000537332.2:c.562dup	ENSP00000444198.2:p.Ser188PhefsTer?
ENST00000618718.1:c.476+71dup	ENSP00000479918.1:n.476+71dup
NM_001168388.2:c.547dup	NP_001161860.1:p.Ser183PhefsTer?
NM_001168389.2:c.562dup	NP_001161861.2:p.Ser188PhefsTer?
NM_006079.4:c.547dup	NP_006070.2:p.Ser183PhefsTer?
NM_006079.5:c.547dup MANE Select	NP_006070.2:p.Ser183PhefsTer?
NM_001168388.3:c.547dup	NP_001161860.1:p.Ser183PhefsTer?
NM_001168389.3:c.562dup	NP_001161861.2:p.Ser188PhefsTer?