Canonical Allele Identifier: CA303988701

Gene: ARID3A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.950380G>T , CM000681.2:g.950380G>T	GRCh38
NC_000019.9:g.950380G>T , CM000681.1:g.950380G>T	GRCh37
NC_000019.8:g.901380G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263620.8:c.694-9712G>T MANE Select	ENSP00000263620.2:n.694-9712G>T
ENST00000263620.7:c.694-9712G>T	ENSP00000263620.2:n.694-9712G>T
ENST00000457152.3:c.179-9712G>T
ENST00000587532.5:c.235-9712G>T	ENSP00000464969.3:n.235-9712G>T
NM_005224.2:c.694-9712G>T	NP_005215.1:n.694-9712G>T
XM_005259513.3:c.694-9712G>T	XP_005259570.1:n.694-9712G>T
XM_005259514.3:c.694-9712G>T	XP_005259571.1:n.694-9712G>T
XM_005259513.5:c.694-9712G>T	XP_005259570.1:n.694-9712G>T
XM_005259514.4:c.694-9712G>T	XP_005259571.1:n.694-9712G>T
XM_017026445.1:c.694-9712G>T	XP_016881934.1:n.694-9712G>T
XM_017026446.1:c.-60-9712G>T	XP_016881935.1:n.-60-9712G>T
XM_024451407.1:c.-60-9712G>T	XP_024307175.1:n.-60-9712G>T
NM_005224.3:c.694-9712G>T MANE Select	NP_005215.1:n.694-9712G>T