Canonical Allele Identifier: CA604811922

Gene: ARID2

Linked Data

• dbSNP Id: rs1249866206
• gnomAD v2: 12-46246615-TAGA-T
• gnomAD v4: 12-45852832-TAGA-T
• MyVariant Identifiers: chr12:g.46246616_46246618del (hg19) ; chr12:g.45852833_45852835del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45852834_45852836del , CM000674.2:g.45852834_45852836del	GRCh38
NC_000012.11:g.46246617_46246619del , CM000674.1:g.46246617_46246619del	GRCh37
NC_000012.10:g.44532884_44532886del	NCBI36
NG_052800.1:g.128170_128172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.4711_4713del	ENSP00000415650.3:p.Glu1571del
ENST00000457135.2:c.920_922del
ENST00000334344.11:c.4711_4713del MANE Select	ENSP00000335044.6:p.Glu1571del
ENST00000422737.6:c.4632_4634del
ENST00000334344.10:c.4711_4713del	ENSP00000335044.6:p.Glu1571del
ENST00000422737.5:c.4264_4266del	ENSP00000415650.1:p.Glu1422del
ENST00000444670.5:c.3541_3543del	ENSP00000397307.1:p.Glu1181del
ENST00000457135.1:c.535_537del	ENSP00000388357.1:p.Glu179del
ENST00000479608.5:n.4002_4004del
NM_152641.2:c.4711_4713del	NP_689854.2:p.Glu1571del
XM_006719272.2:c.4711_4713del	XP_006719335.1:p.Glu1571del
XM_011538025.1:c.3079_3081del	XP_011536327.1:p.Glu1027del
XR_944505.1:n.4859_4861del
NM_001347839.1:c.4711_4713del	NP_001334768.1:p.Glu1571del
NM_152641.3:c.4711_4713del	NP_689854.2:p.Glu1571del
XM_006719272.4:c.4711_4713del	XP_006719335.1:p.Glu1571del
XR_944505.3:n.4842_4844del
NM_152641.4:c.4711_4713del MANE Select	NP_689854.2:p.Glu1571del
NM_001347839.2:c.4711_4713del	NP_001334768.1:p.Glu1571del