Canonical Allele Identifier: CA394799152

Gene: GRIN2A

Linked Data

• COSMIC: COSM3730394
• MyVariant Identifiers: chr16:g.9923307G>C (hg19) ; chr16:g.9829450G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9829450G>C , CM000678.2:g.9829450G>C	GRCh38
NC_000016.9:g.9923307G>C , CM000678.1:g.9923307G>C	GRCh37
NC_000016.8:g.9830808G>C	NCBI36
NG_011812.1:g.358305C>G
NG_011812.2:g.358305C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1980C>G MANE Select	ENSP00000332549.3:p.Asp660Glu
ENST00000535259.6:c.1509C>G	ENSP00000441572.3:p.Asp503Glu
ENST00000636273.2:n.1573C>G
ENST00000674742.1:c.1509C>G	ENSP00000502200.1:p.Asp503Glu
ENST00000675398.1:c.1980C>G	ENSP00000502752.1:p.Asp660Glu
ENST00000330684.3:c.1980C>G	ENSP00000332549.3:p.Asp660Glu
ENST00000396573.6:c.1980C>G	ENSP00000379818.2:p.Asp660Glu
ENST00000396575.6:c.1569C>G	ENSP00000379820.3:p.Asp523Glu
ENST00000461292.3:n.1619C>G
ENST00000535259.5:c.1569C>G	ENSP00000441572.2:p.Asp523Glu
ENST00000562109.5:c.1980C>G	ENSP00000454998.1:p.Asp660Glu
NM_000833.4:c.1980C>G	NP_000824.1:p.Asp660Glu
NM_001134407.2:c.1980C>G	NP_001127879.1:p.Asp660Glu
NM_001134408.2:c.1980C>G	NP_001127880.1:p.Asp660Glu
XM_011522456.1:c.1821C>G	XP_011520758.1:p.Asp607Glu
XM_011522457.1:c.1722C>G	XP_011520759.1:p.Asp574Glu
XM_011522458.1:c.1509C>G	XP_011520760.1:p.Asp503Glu
XM_011522459.1:c.1509C>G	XP_011520761.1:p.Asp503Glu
XM_011522460.1:c.1509C>G	XP_011520762.1:p.Asp503Glu
XM_011522461.1:c.1980C>G	XP_011520763.1:p.Asp660Glu
XM_011522458.3:c.1509C>G	XP_011520760.1:p.Asp503Glu
XM_011522461.3:c.1980C>G	XP_011520763.1:p.Asp660Glu
XM_017023172.1:c.2136C>G	XP_016878661.1:p.Asp712Glu
XM_017023173.1:c.2136C>G	XP_016878662.1:p.Asp712Glu
NM_001134407.3:c.1980C>G MANE Select	NP_001127879.1:p.Asp660Glu
NM_000833.5:c.1980C>G	NP_000824.1:p.Asp660Glu