Canonical Allele Identifier: CA394706016

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141126295
• MyVariant Identifiers: chr16:g.9857268A>T (hg19) ; chr16:g.9763411A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763411A>T , CM000678.2:g.9763411A>T	GRCh38
NC_000016.9:g.9857268A>T , CM000678.1:g.9857268A>T	GRCh37
NC_000016.8:g.9764769A>T	NCBI36
NG_011812.1:g.424344T>A
NG_011812.2:g.424344T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4133T>A MANE Select	ENSP00000332549.3:p.Val1378Asp
ENST00000535259.6:c.3319T>A	ENSP00000441572.3:p.Leu1107Ile
ENST00000636273.2:n.3383T>A
ENST00000674742.1:c.3662T>A	ENSP00000502200.1:p.Val1221Asp
ENST00000675398.1:c.*1503T>A	ENSP00000502752.1:n.*1503T>A
ENST00000330684.3:c.4133T>A	ENSP00000332549.3:p.Val1378Asp
ENST00000396573.6:c.4133T>A	ENSP00000379818.2:p.Val1378Asp
ENST00000396575.6:c.3722T>A	ENSP00000379820.3:p.Val1241Asp
ENST00000461292.3:n.3429T>A
ENST00000535259.5:c.3379T>A	ENSP00000441572.2:p.Leu1127Ile
ENST00000562109.5:c.3790T>A	ENSP00000454998.1:p.Leu1264Ile
NM_000833.4:c.4133T>A	NP_000824.1:p.Val1378Asp
NM_001134407.2:c.4133T>A	NP_001127879.1:p.Val1378Asp
NM_001134408.2:c.3790T>A	NP_001127880.1:p.Leu1264Ile
XM_011522456.1:c.3974T>A	XP_011520758.1:p.Val1325Asp
XM_011522457.1:c.3875T>A	XP_011520759.1:p.Val1292Asp
XM_011522458.1:c.3662T>A	XP_011520760.1:p.Val1221Asp
XM_011522459.1:c.3662T>A	XP_011520761.1:p.Val1221Asp
XM_011522460.1:c.3662T>A	XP_011520762.1:p.Val1221Asp
XM_011522461.1:c.3790T>A	XP_011520763.1:p.Leu1264Ile
XM_011522458.3:c.3662T>A	XP_011520760.1:p.Val1221Asp
XM_011522461.3:c.3790T>A	XP_011520763.1:p.Leu1264Ile
XM_017023172.1:c.4289T>A	XP_016878661.1:p.Val1430Asp
XM_017023173.1:c.3946T>A	XP_016878662.1:p.Leu1316Ile
NM_001134407.3:c.4133T>A MANE Select	NP_001127879.1:p.Val1378Asp
NM_000833.5:c.4133T>A	NP_000824.1:p.Val1378Asp