Canonical Allele Identifier: CA493693254

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141136542
• MyVariant Identifiers: chr16:g.9858551C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764694C>T , CM000678.2:g.9764694C>T	GRCh38
NC_000016.9:g.9858551C>T , CM000678.1:g.9858551C>T	GRCh37
NC_000016.8:g.9766052C>T	NCBI36
NG_011812.1:g.423061G>A
NG_011812.2:g.423061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2850G>A MANE Select	ENSP00000332549.3:p.Gln950=
ENST00000535259.6:c.2379G>A	ENSP00000441572.3:p.Gln793=
ENST00000636273.2:n.2443G>A
ENST00000674742.1:c.2379G>A	ENSP00000502200.1:p.Gln793=
ENST00000675398.1:c.*220G>A	ENSP00000502752.1:n.*220G>A
ENST00000330684.3:c.2850G>A	ENSP00000332549.3:p.Gln950=
ENST00000396573.6:c.2850G>A	ENSP00000379818.2:p.Gln950=
ENST00000396575.6:c.2439G>A	ENSP00000379820.3:p.Gln813=
ENST00000461292.3:n.2489G>A
ENST00000535259.5:c.2439G>A	ENSP00000441572.2:p.Gln813=
ENST00000562109.5:c.2850G>A	ENSP00000454998.1:p.Gln950=
NM_000833.4:c.2850G>A	NP_000824.1:p.Gln950=
NM_001134407.2:c.2850G>A	NP_001127879.1:p.Gln950=
NM_001134408.2:c.2850G>A	NP_001127880.1:p.Gln950=
XM_011522456.1:c.2691G>A	XP_011520758.1:p.Gln897=
XM_011522457.1:c.2592G>A	XP_011520759.1:p.Gln864=
XM_011522458.1:c.2379G>A	XP_011520760.1:p.Gln793=
XM_011522459.1:c.2379G>A	XP_011520761.1:p.Gln793=
XM_011522460.1:c.2379G>A	XP_011520762.1:p.Gln793=
XM_011522461.1:c.2850G>A	XP_011520763.1:p.Gln950=
XM_011522458.3:c.2379G>A	XP_011520760.1:p.Gln793=
XM_011522461.3:c.2850G>A	XP_011520763.1:p.Gln950=
XM_017023172.1:c.3006G>A	XP_016878661.1:p.Gln1002=
XM_017023173.1:c.3006G>A	XP_016878662.1:p.Gln1002=
NM_001134407.3:c.2850G>A MANE Select	NP_001127879.1:p.Gln950=
NM_000833.5:c.2850G>A	NP_000824.1:p.Gln950=