Canonical Allele Identifier: CA1667372365

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373384_139373408delinsCGCGCCGCCGCCCGAGCTGCTGCCA , CM000668.2:g.139373384_139373408delinsCGCGCCGCCGCCCGAGCTGCTGCCA	GRCh38
NC_000006.11:g.139694521_139694545delinsCGCGCCGCCGCCCGAGCTGCTGCCA , CM000668.1:g.139694521_139694545delinsCGCGCCGCCGCCCGAGCTGCTGCCA	GRCh37
NC_000006.10:g.139736214_139736238delinsCGCGCCGCCGCCCGAGCTGCTGCCA	NCBI36
NG_016169.1:g.6241_6265delinsTGGCAGCAGCTCGGGCGGCGGCGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG MANE Select	ENSP00000356623.2:p.Ser179=
ENST00000367651.3:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG	ENSP00000356623.2:p.Ser179=
ENST00000536159.2:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG	ENSP00000442831.1:p.Ser179=
ENST00000537332.2:c.552_576delinsTGGCAGCAGCTCGGGCGGCGGCGCG	ENSP00000444198.2:p.Ser184=
ENST00000618718.1:c.476+61_476+85delinsTGGCAGCAGCTCGGGCGGCGGCGCG	ENSP00000479918.1:n.476+61_476+85delinsTGGCAGCAGCTCGGGCGGCGGC...
NM_001168388.2:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG	NP_001161860.1:p.Ser179=
NM_001168389.2:c.552_576delinsTGGCAGCAGCTCGGGCGGCGGCGCG	NP_001161861.2:p.Ser184=
NM_006079.4:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG	NP_006070.2:p.Ser179=
NM_006079.5:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG MANE Select	NP_006070.2:p.Ser179=
NM_001168388.3:c.537_561delinsTGGCAGCAGCTCGGGCGGCGGCGCG	NP_001161860.1:p.Ser179=
NM_001168389.3:c.552_576delinsTGGCAGCAGCTCGGGCGGCGGCGCG	NP_001161861.2:p.Ser184=