Canonical Allele Identifier: CA7204782

Gene: ARID4A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.58365301G>A , CM000676.2:g.58365301G>A	GRCh38
NC_000014.8:g.58832019G>A , CM000676.1:g.58832019G>A	GRCh37
NC_000014.7:g.57901772G>A	NCBI36
NG_052999.1:g.71917G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002892.4:c.3211+1G>A MANE Select	NP_002883.3:n.3211+1G>A
ENST00000355431.8:c.3211+1G>A MANE Select	ENSP00000347602.3:n.3211+1G>A
NM_002892.3:c.3211+1G>A	NP_002883.3:n.3211+1G>A
NM_023000.2:c.3211+1G>A	NP_075376.2:n.3211+1G>A
NM_023000.3:c.3211+1G>A	NP_075376.2:n.3211+1G>A
NM_023001.2:c.3211+1G>A	NP_075377.2:n.3211+1G>A
NM_023001.3:c.3211+1G>A	NP_075377.2:n.3211+1G>A
ENST00000348476.7:c.3211+1G>A	ENSP00000344556.3:n.3211+1G>A
ENST00000355431.7:c.3211+1G>A	ENSP00000347602.3:n.3211+1G>A
ENST00000395168.7:c.3211+1G>A	ENSP00000378597.3:n.3211+1G>A
ENST00000431317.6:c.3211+1G>A	ENSP00000397368.2:n.3211+1G>A
XM_005267964.1:c.3271+1G>A	XP_005268021.1:n.3271+1G>A
XM_005267964.2:c.3271+1G>A	XP_005268021.1:n.3271+1G>A
XM_005267965.1:c.3271+1G>A	XP_005268022.1:n.3271+1G>A
XM_005267965.2:c.3271+1G>A	XP_005268022.1:n.3271+1G>A
XM_011537054.1:c.3271+1G>A	XP_011535356.1:n.3271+1G>A
XM_011537055.1:c.2998+1G>A	XP_011535357.1:n.2998+1G>A
XM_011537056.1:c.2305+1G>A	XP_011535358.1:n.2305+1G>A
XM_017021560.1:c.3272G>A	XP_016877049.1:p.Gly1091Asp
XM_017021561.1:c.3272G>A	XP_016877050.1:p.Gly1091Asp
XM_017021562.1:c.3212G>A	XP_016877051.1:p.Gly1071Asp
XM_017021563.1:c.3272G>A	XP_016877052.1:p.Gly1091Asp
XM_017021564.1:c.2831G>A	XP_016877053.1:p.Gly944Asp
XM_017021565.1:c.2245+1G>A	XP_016877054.1:n.2245+1G>A
XM_024449683.1:c.1565G>A	XP_024305451.1:p.Gly522Asp
XM_024449684.1:c.1505G>A	XP_024305452.1:p.Gly502Asp