Canonical Allele Identifier: CA2631674848

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9763377-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763378dup , CM000678.2:g.9763378dup	GRCh38
NC_000016.9:g.9857235dup , CM000678.1:g.9857235dup	GRCh37
NC_000016.8:g.9764736dup	NCBI36
NG_011812.1:g.424377dup
NG_011812.2:g.424377dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4166dup MANE Select	ENSP00000332549.3:p.His1389GlnfsTer10
ENST00000535259.6:c.3352dup	ENSP00000441572.3:p.Thr1118AsnfsTer?
ENST00000636273.2:n.3416dup
ENST00000674742.1:c.3695dup	ENSP00000502200.1:p.His1232GlnfsTer10
ENST00000675398.1:c.*1536dup	ENSP00000502752.1:n.*1536dup
ENST00000330684.3:c.4166dup	ENSP00000332549.3:p.His1389GlnfsTer10
ENST00000396573.6:c.4166dup	ENSP00000379818.2:p.His1389GlnfsTer10
ENST00000396575.6:c.3755dup	ENSP00000379820.3:p.His1252GlnfsTer10
ENST00000461292.3:n.3462dup
ENST00000535259.5:c.3412dup	ENSP00000441572.2:p.Thr1138AsnfsTer?
ENST00000562109.5:c.3823dup	ENSP00000454998.1:p.Thr1275AsnfsTer?
NM_000833.4:c.4166dup	NP_000824.1:p.His1389GlnfsTer10
NM_001134407.2:c.4166dup	NP_001127879.1:p.His1389GlnfsTer10
NM_001134408.2:c.3823dup	NP_001127880.1:p.Thr1275AsnfsTer?
XM_011522456.1:c.4007dup	XP_011520758.1:p.His1336GlnfsTer10
XM_011522457.1:c.3908dup	XP_011520759.1:p.His1303GlnfsTer10
XM_011522458.1:c.3695dup	XP_011520760.1:p.His1232GlnfsTer10
XM_011522459.1:c.3695dup	XP_011520761.1:p.His1232GlnfsTer10
XM_011522460.1:c.3695dup	XP_011520762.1:p.His1232GlnfsTer10
XM_011522461.1:c.3823dup	XP_011520763.1:p.Thr1275AsnfsTer?
XM_011522458.3:c.3695dup	XP_011520760.1:p.His1232GlnfsTer10
XM_011522461.3:c.3823dup	XP_011520763.1:p.Thr1275AsnfsTer?
XM_017023172.1:c.4322dup	XP_016878661.1:p.His1441GlnfsTer10
XM_017023173.1:c.3979dup	XP_016878662.1:p.Thr1327AsnfsTer?
NM_001134407.3:c.4166dup MANE Select	NP_001127879.1:p.His1389GlnfsTer10
NM_000833.5:c.4166dup	NP_000824.1:p.His1389GlnfsTer10