Canonical Allele Identifier: CA394799744

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 1453886
• ClinVar RCV Id: RCV001960520
• dbSNP Id: rs2141312814
• MyVariant Identifiers: chr16:g.9923456G>T (hg19) ; chr16:g.9829599G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9829599G>T , CM000678.2:g.9829599G>T	GRCh38
NC_000016.9:g.9923456G>T , CM000678.1:g.9923456G>T	GRCh37
NC_000016.8:g.9830957G>T	NCBI36
NG_011812.1:g.358156C>A
NG_011812.2:g.358156C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.1831C>A MANE Select	ENSP00000332549.3:p.Leu611Met
ENST00000535259.6:c.1360C>A	ENSP00000441572.3:p.Leu454Met
ENST00000636273.2:n.1424C>A
ENST00000674742.1:c.1360C>A	ENSP00000502200.1:p.Leu454Met
ENST00000675398.1:c.1831C>A	ENSP00000502752.1:p.Leu611Met
ENST00000330684.3:c.1831C>A	ENSP00000332549.3:p.Leu611Met
ENST00000396573.6:c.1831C>A	ENSP00000379818.2:p.Leu611Met
ENST00000396575.6:c.1420C>A	ENSP00000379820.3:p.Leu474Met
ENST00000461292.3:n.1470C>A
ENST00000535259.5:c.1420C>A	ENSP00000441572.2:p.Leu474Met
ENST00000562109.5:c.1831C>A	ENSP00000454998.1:p.Leu611Met
NM_000833.4:c.1831C>A	NP_000824.1:p.Leu611Met
NM_001134407.2:c.1831C>A	NP_001127879.1:p.Leu611Met
NM_001134408.2:c.1831C>A	NP_001127880.1:p.Leu611Met
XM_011522456.1:c.1672C>A	XP_011520758.1:p.Leu558Met
XM_011522457.1:c.1573C>A	XP_011520759.1:p.Leu525Met
XM_011522458.1:c.1360C>A	XP_011520760.1:p.Leu454Met
XM_011522459.1:c.1360C>A	XP_011520761.1:p.Leu454Met
XM_011522460.1:c.1360C>A	XP_011520762.1:p.Leu454Met
XM_011522461.1:c.1831C>A	XP_011520763.1:p.Leu611Met
XM_011522458.3:c.1360C>A	XP_011520760.1:p.Leu454Met
XM_011522461.3:c.1831C>A	XP_011520763.1:p.Leu611Met
XM_017023172.1:c.1987C>A	XP_016878661.1:p.Leu663Met
XM_017023173.1:c.1987C>A	XP_016878662.1:p.Leu663Met
NM_001134407.3:c.1831C>A MANE Select	NP_001127879.1:p.Leu611Met
NM_000833.5:c.1831C>A	NP_000824.1:p.Leu611Met