Canonical Allele Identifier: CA493693446

Gene: GRIN2A

Linked Data

• dbSNP Id: rs570907044
• MyVariant Identifiers: chr16:g.9858590A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764733A>G , CM000678.2:g.9764733A>G	GRCh38
NC_000016.9:g.9858590A>G , CM000678.1:g.9858590A>G	GRCh37
NC_000016.8:g.9766091A>G	NCBI36
NG_011812.1:g.423022T>C
NG_011812.2:g.423022T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2811T>C MANE Select	ENSP00000332549.3:p.Asp937=
ENST00000535259.6:c.2340T>C	ENSP00000441572.3:p.Asp780=
ENST00000636273.2:n.2404T>C
ENST00000674742.1:c.2340T>C	ENSP00000502200.1:p.Asp780=
ENST00000675398.1:c.*181T>C	ENSP00000502752.1:n.*181T>C
ENST00000330684.3:c.2811T>C	ENSP00000332549.3:p.Asp937=
ENST00000396573.6:c.2811T>C	ENSP00000379818.2:p.Asp937=
ENST00000396575.6:c.2400T>C	ENSP00000379820.3:p.Asp800=
ENST00000461292.3:n.2450T>C
ENST00000535259.5:c.2400T>C	ENSP00000441572.2:p.Asp800=
ENST00000562109.5:c.2811T>C	ENSP00000454998.1:p.Asp937=
NM_000833.4:c.2811T>C	NP_000824.1:p.Asp937=
NM_001134407.2:c.2811T>C	NP_001127879.1:p.Asp937=
NM_001134408.2:c.2811T>C	NP_001127880.1:p.Asp937=
XM_011522456.1:c.2652T>C	XP_011520758.1:p.Asp884=
XM_011522457.1:c.2553T>C	XP_011520759.1:p.Asp851=
XM_011522458.1:c.2340T>C	XP_011520760.1:p.Asp780=
XM_011522459.1:c.2340T>C	XP_011520761.1:p.Asp780=
XM_011522460.1:c.2340T>C	XP_011520762.1:p.Asp780=
XM_011522461.1:c.2811T>C	XP_011520763.1:p.Asp937=
XM_011522458.3:c.2340T>C	XP_011520760.1:p.Asp780=
XM_011522461.3:c.2811T>C	XP_011520763.1:p.Asp937=
XM_017023172.1:c.2967T>C	XP_016878661.1:p.Asp989=
XM_017023173.1:c.2967T>C	XP_016878662.1:p.Asp989=
NM_001134407.3:c.2811T>C MANE Select	NP_001127879.1:p.Asp937=
NM_000833.5:c.2811T>C	NP_000824.1:p.Asp937=