Canonical Allele Identifier: CA2773276765

Gene: CITED2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.139373407_139373408insCGC , CM000668.2:g.139373407_139373408insCGC	GRCh38
NC_000006.11:g.139694544_139694545insCGC , CM000668.1:g.139694544_139694545insCGC	GRCh37
NC_000006.10:g.139736237_139736238insCGC	NCBI36
NG_016169.1:g.6242_6243insCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367651.4:c.538_539insCGG MANE Select	ENSP00000356623.2:p.Ser179_Gly180insAla
ENST00000367651.3:c.538_539insCGG	ENSP00000356623.2:p.Ser179_Gly180insAla
ENST00000536159.2:c.538_539insCGG	ENSP00000442831.1:p.Ser179_Gly180insAla
ENST00000537332.2:c.553_554insCGG	ENSP00000444198.2:p.Ser184_Gly185insAla
ENST00000618718.1:c.476+62_476+63insCGG	ENSP00000479918.1:n.476+62_476+63insCGG
NM_001168388.2:c.538_539insCGG	NP_001161860.1:p.Ser179_Gly180insAla
NM_001168389.2:c.553_554insCGG	NP_001161861.2:p.Ser184_Gly185insAla
NM_006079.4:c.538_539insCGG	NP_006070.2:p.Ser179_Gly180insAla
NM_006079.5:c.538_539insCGG MANE Select	NP_006070.2:p.Ser179_Gly180insAla
NM_001168388.3:c.538_539insCGG	NP_001161860.1:p.Ser179_Gly180insAla
NM_001168389.3:c.553_554insCGG	NP_001161861.2:p.Ser184_Gly185insAla