Canonical Allele Identifier: CA2033475756

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852754_45852774delinsCCAACAATGCTGGCTGCAGCG , CM000674.2:g.45852754_45852774delinsCCAACAATGCTGGCTGCAGCG	GRCh38
NC_000012.11:g.46246537_46246557delinsCCAACAATGCTGGCTGCAGCG , CM000674.1:g.46246537_46246557delinsCCAACAATGCTGGCTGCAGCG	GRCh37
NC_000012.10:g.44532804_44532824delinsCCAACAATGCTGGCTGCAGCG	NCBI36
NG_052800.1:g.128090_128110delinsCCAACAATGCTGGCTGCAGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	ENSP00000415650.3:p.Pro1544=
ENST00000457135.2:c.840_860delinsCCAACAATGCTGGCTGCAGCG
ENST00000334344.11:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG MANE Select	ENSP00000335044.6:p.Pro1544=
ENST00000422737.6:c.4552_4572delinsCCAACAATGCTGGCTGCAGCG
ENST00000334344.10:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	ENSP00000335044.6:p.Pro1544=
ENST00000422737.5:c.4184_4204delinsCCAACAATGCTGGCTGCAGCG	ENSP00000415650.1:p.Pro1395=
ENST00000444670.5:c.3461_3481delinsCCAACAATGCTGGCTGCAGCG	ENSP00000397307.1:p.Pro1154=
ENST00000457135.1:c.455_475delinsCCAACAATGCTGGCTGCAGCG	ENSP00000388357.1:p.Pro152=
ENST00000479608.5:n.3922_3942delinsCCAACAATGCTGGCTGCAGCG
NM_152641.2:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	NP_689854.2:p.Pro1544=
XM_006719272.2:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	XP_006719335.1:p.Pro1544=
XM_011538025.1:c.2999_3019delinsCCAACAATGCTGGCTGCAGCG	XP_011536327.1:p.Pro1000=
XR_944505.1:n.4779_4799delinsCCAACAATGCTGGCTGCAGCG
NM_001347839.1:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	NP_001334768.1:p.Pro1544=
NM_152641.3:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	NP_689854.2:p.Pro1544=
XM_006719272.4:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	XP_006719335.1:p.Pro1544=
XR_944505.3:n.4762_4782delinsCCAACAATGCTGGCTGCAGCG
NM_152641.4:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG MANE Select	NP_689854.2:p.Pro1544=
NM_001347839.2:c.4631_4651delinsCCAACAATGCTGGCTGCAGCG	NP_001334768.1:p.Pro1544=