Canonical Allele Identifier: CA394798163

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031878C>G (hg19) ; chr16:g.9938021C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938021C>G , CM000678.2:g.9938021C>G	GRCh38
NC_000016.9:g.10031878C>G , CM000678.1:g.10031878C>G	GRCh37
NC_000016.8:g.9939379C>G	NCBI36
NG_011812.1:g.249734G>C
NG_011812.2:g.249734G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.945G>C MANE Select	ENSP00000332549.3:p.Glu315Asp
ENST00000535259.6:c.474G>C	ENSP00000441572.3:p.Glu158Asp
ENST00000636273.2:n.538G>C
ENST00000637393.1:c.537G>C	ENSP00000490232.1:p.Glu179Asp
ENST00000674742.1:c.474G>C	ENSP00000502200.1:p.Glu158Asp
ENST00000675189.1:n.1429G>C
ENST00000675398.1:c.945G>C	ENSP00000502752.1:p.Glu315Asp
ENST00000330684.3:c.945G>C	ENSP00000332549.3:p.Glu315Asp
ENST00000396573.6:c.945G>C	ENSP00000379818.2:p.Glu315Asp
ENST00000396575.6:c.534G>C	ENSP00000379820.3:p.Glu178Asp
ENST00000461292.3:n.584G>C
ENST00000535259.5:c.534G>C	ENSP00000441572.2:p.Glu178Asp
ENST00000562109.5:c.945G>C	ENSP00000454998.1:p.Glu315Asp
ENST00000566683.1:n.241-46921G>C
ENST00000568247.3:n.837G>C
NM_000833.4:c.945G>C	NP_000824.1:p.Glu315Asp
NM_001134407.2:c.945G>C	NP_001127879.1:p.Glu315Asp
NM_001134408.2:c.945G>C	NP_001127880.1:p.Glu315Asp
XM_011522456.1:c.786G>C	XP_011520758.1:p.Glu262Asp
XM_011522457.1:c.687G>C	XP_011520759.1:p.Glu229Asp
XM_011522458.1:c.474G>C	XP_011520760.1:p.Glu158Asp
XM_011522459.1:c.474G>C	XP_011520761.1:p.Glu158Asp
XM_011522460.1:c.474G>C	XP_011520762.1:p.Glu158Asp
XM_011522461.1:c.945G>C	XP_011520763.1:p.Glu315Asp
XM_011522458.3:c.474G>C	XP_011520760.1:p.Glu158Asp
XM_011522461.3:c.945G>C	XP_011520763.1:p.Glu315Asp
XM_017023172.1:c.1101G>C	XP_016878661.1:p.Glu367Asp
XM_017023173.1:c.1101G>C	XP_016878662.1:p.Glu367Asp
NM_001134407.3:c.945G>C MANE Select	NP_001127879.1:p.Glu315Asp
NM_000833.5:c.945G>C	NP_000824.1:p.Glu315Asp