Canonical Allele Identifier: CA394797869

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9822359-C-G
• MyVariant Identifiers: chr16:g.9916216C>G (hg19) ; chr16:g.9822359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9822359C>G , CM000678.2:g.9822359C>G	GRCh38
NC_000016.9:g.9916216C>G , CM000678.1:g.9916216C>G	GRCh37
NC_000016.8:g.9823717C>G	NCBI36
NG_011812.1:g.365396G>C
NG_011812.2:g.365396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2073G>C MANE Select	ENSP00000332549.3:p.Glu691Asp
ENST00000535259.6:c.1602G>C	ENSP00000441572.3:p.Glu534Asp
ENST00000636273.2:n.1666G>C
ENST00000674742.1:c.1602G>C	ENSP00000502200.1:p.Glu534Asp
ENST00000675398.1:c.2073G>C	ENSP00000502752.1:p.Glu691Asp
ENST00000330684.3:c.2073G>C	ENSP00000332549.3:p.Glu691Asp
ENST00000396573.6:c.2073G>C	ENSP00000379818.2:p.Glu691Asp
ENST00000396575.6:c.1662G>C	ENSP00000379820.3:p.Glu554Asp
ENST00000461292.3:n.1712G>C
ENST00000535259.5:c.1662G>C	ENSP00000441572.2:p.Glu554Asp
ENST00000562109.5:c.2073G>C	ENSP00000454998.1:p.Glu691Asp
NM_000833.4:c.2073G>C	NP_000824.1:p.Glu691Asp
NM_001134407.2:c.2073G>C	NP_001127879.1:p.Glu691Asp
NM_001134408.2:c.2073G>C	NP_001127880.1:p.Glu691Asp
XM_011522456.1:c.1914G>C	XP_011520758.1:p.Glu638Asp
XM_011522457.1:c.1815G>C	XP_011520759.1:p.Glu605Asp
XM_011522458.1:c.1602G>C	XP_011520760.1:p.Glu534Asp
XM_011522459.1:c.1602G>C	XP_011520761.1:p.Glu534Asp
XM_011522460.1:c.1602G>C	XP_011520762.1:p.Glu534Asp
XM_011522461.1:c.2073G>C	XP_011520763.1:p.Glu691Asp
XM_011522458.3:c.1602G>C	XP_011520760.1:p.Glu534Asp
XM_011522461.3:c.2073G>C	XP_011520763.1:p.Glu691Asp
XM_017023172.1:c.2229G>C	XP_016878661.1:p.Glu743Asp
XM_017023173.1:c.2229G>C	XP_016878662.1:p.Glu743Asp
NM_001134407.3:c.2073G>C MANE Select	NP_001127879.1:p.Glu691Asp
NM_000833.5:c.2073G>C	NP_000824.1:p.Glu691Asp