Canonical Allele Identifier: CA384455536

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45837656G>C , CM000674.2:g.45837656G>C	GRCh38
NC_000012.11:g.46231439G>C , CM000674.1:g.46231439G>C	GRCh37
NC_000012.10:g.44517706G>C	NCBI36
NG_052800.1:g.112992G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.1279G>C	ENSP00000415650.3:p.Glu427Gln
ENST00000334344.11:c.1279G>C MANE Select	ENSP00000335044.6:p.Glu427Gln
ENST00000422737.6:c.1200G>C
ENST00000334344.10:c.1279G>C	ENSP00000335044.6:p.Glu427Gln
ENST00000422737.5:c.832G>C	ENSP00000415650.1:p.Glu278Gln
ENST00000444670.5:c.166G>C	ENSP00000397307.1:p.Glu56Gln
ENST00000479608.5:n.487G>C
ENST00000480128.1:n.303G>C
NM_152641.2:c.1279G>C	NP_689854.2:p.Glu427Gln
XM_006719272.2:c.1279G>C	XP_006719335.1:p.Glu427Gln
XM_011538025.1:c.-437G>C	XP_011536327.1:n.-437G>C
XR_944505.1:n.1427G>C
XR_944892.1:n.289+2196C>G
XR_944893.1:n.289+2196C>G
NM_001347839.1:c.1279G>C	NP_001334768.1:p.Glu427Gln
NM_152641.3:c.1279G>C	NP_689854.2:p.Glu427Gln
XM_006719272.4:c.1279G>C	XP_006719335.1:p.Glu427Gln
XR_001749098.1:n.476+2196C>G
XR_944505.3:n.1410G>C
XR_944892.2:n.289+2196C>G
NM_152641.4:c.1279G>C MANE Select	NP_689854.2:p.Glu427Gln
NM_001347839.2:c.1279G>C	NP_001334768.1:p.Glu427Gln