Canonical Allele Identifier: CA10603254

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45839336_45839339del , CM000674.2:g.45839336_45839339del	GRCh38
NC_000012.11:g.46233119_46233122del , CM000674.1:g.46233119_46233122del	GRCh37
NC_000012.10:g.44519386_44519389del	NCBI36
NG_052800.1:g.114672_114675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.1338_1341del	ENSP00000415650.3:p.Leu446PhefsTer16
ENST00000334344.11:c.1338_1341del MANE Select	ENSP00000335044.6:p.Leu446PhefsTer16
ENST00000422737.6:c.1259_1262del
ENST00000334344.10:c.1338_1341del	ENSP00000335044.6:p.Leu446PhefsTer16
ENST00000422737.5:c.891_894del	ENSP00000415650.1:p.Leu297PhefsTer16
ENST00000444670.5:c.218-50_218-47del	ENSP00000397307.1:n.218-50_218-47del
ENST00000479608.5:n.546_549del
ENST00000480128.1:n.362_365del
NM_152641.2:c.1338_1341del	NP_689854.2:p.Leu446PhefsTer16
XM_006719272.2:c.1338_1341del	XP_006719335.1:p.Leu446PhefsTer16
XM_011538025.1:c.-378_-375del	XP_011536327.1:n.-378_-375del
XR_944505.1:n.1486_1489del
XR_944892.1:n.289+513_289+516del
XR_944893.1:n.289+513_289+516del
NM_001347839.1:c.1338_1341del	NP_001334768.1:p.Leu446PhefsTer16
NM_152641.3:c.1338_1341del	NP_689854.2:p.Leu446PhefsTer16
XM_006719272.4:c.1338_1341del	XP_006719335.1:p.Leu446PhefsTer16
XR_001749098.1:n.476+513_476+516del
XR_944505.3:n.1469_1472del
XR_944892.2:n.289+513_289+516del
NM_152641.4:c.1338_1341del MANE Select	NP_689854.2:p.Leu446PhefsTer16
NM_001347839.2:c.1338_1341del	NP_001334768.1:p.Leu446PhefsTer16