Canonical Allele Identifier: CA384459551

Gene: ARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.45839469A>T , CM000674.2:g.45839469A>T	GRCh38
NC_000012.11:g.46233252A>T , CM000674.1:g.46233252A>T	GRCh37
NC_000012.10:g.44519519A>T	NCBI36
NG_052800.1:g.114805A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422737.7:c.1471A>T	ENSP00000415650.3:p.Thr491Ser
ENST00000334344.11:c.1471A>T MANE Select	ENSP00000335044.6:p.Thr491Ser
ENST00000422737.6:c.1392A>T
ENST00000334344.10:c.1471A>T	ENSP00000335044.6:p.Thr491Ser
ENST00000422737.5:c.1024A>T	ENSP00000415650.1:p.Thr342Ser
ENST00000444670.5:c.301A>T	ENSP00000397307.1:p.Thr101Ser
ENST00000479608.5:n.679A>T
ENST00000480128.1:n.495A>T
NM_152641.2:c.1471A>T	NP_689854.2:p.Thr491Ser
XM_006719272.2:c.1471A>T	XP_006719335.1:p.Thr491Ser
XM_011538025.1:c.-245A>T	XP_011536327.1:n.-245A>T
XR_944505.1:n.1619A>T
XR_944892.1:n.289+383T>A
XR_944893.1:n.289+383T>A
NM_001347839.1:c.1471A>T	NP_001334768.1:p.Thr491Ser
NM_152641.3:c.1471A>T	NP_689854.2:p.Thr491Ser
XM_006719272.4:c.1471A>T	XP_006719335.1:p.Thr491Ser
XR_001749098.1:n.476+383T>A
XR_944505.3:n.1602A>T
XR_944892.2:n.289+383T>A
NM_152641.4:c.1471A>T MANE Select	NP_689854.2:p.Thr491Ser
NM_001347839.2:c.1471A>T	NP_001334768.1:p.Thr491Ser