Canonical Allele Identifier: CA394706010

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.9857266T>G (hg19) ; chr16:g.9763409T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763409T>G , CM000678.2:g.9763409T>G	GRCh38
NC_000016.9:g.9857266T>G , CM000678.1:g.9857266T>G	GRCh37
NC_000016.8:g.9764767T>G	NCBI36
NG_011812.1:g.424346A>C
NG_011812.2:g.424346A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4135A>C MANE Select	ENSP00000332549.3:p.Ile1379Leu
ENST00000535259.6:c.3321A>C	ENSP00000441572.3:p.Leu1107Phe
ENST00000636273.2:n.3385A>C
ENST00000674742.1:c.3664A>C	ENSP00000502200.1:p.Ile1222Leu
ENST00000675398.1:c.*1505A>C	ENSP00000502752.1:n.*1505A>C
ENST00000330684.3:c.4135A>C	ENSP00000332549.3:p.Ile1379Leu
ENST00000396573.6:c.4135A>C	ENSP00000379818.2:p.Ile1379Leu
ENST00000396575.6:c.3724A>C	ENSP00000379820.3:p.Ile1242Leu
ENST00000461292.3:n.3431A>C
ENST00000535259.5:c.3381A>C	ENSP00000441572.2:p.Leu1127Phe
ENST00000562109.5:c.3792A>C	ENSP00000454998.1:p.Leu1264Phe
NM_000833.4:c.4135A>C	NP_000824.1:p.Ile1379Leu
NM_001134407.2:c.4135A>C	NP_001127879.1:p.Ile1379Leu
NM_001134408.2:c.3792A>C	NP_001127880.1:p.Leu1264Phe
XM_011522456.1:c.3976A>C	XP_011520758.1:p.Ile1326Leu
XM_011522457.1:c.3877A>C	XP_011520759.1:p.Ile1293Leu
XM_011522458.1:c.3664A>C	XP_011520760.1:p.Ile1222Leu
XM_011522459.1:c.3664A>C	XP_011520761.1:p.Ile1222Leu
XM_011522460.1:c.3664A>C	XP_011520762.1:p.Ile1222Leu
XM_011522461.1:c.3792A>C	XP_011520763.1:p.Leu1264Phe
XM_011522458.3:c.3664A>C	XP_011520760.1:p.Ile1222Leu
XM_011522461.3:c.3792A>C	XP_011520763.1:p.Leu1264Phe
XM_017023172.1:c.4291A>C	XP_016878661.1:p.Ile1431Leu
XM_017023173.1:c.3948A>C	XP_016878662.1:p.Leu1316Phe
NM_001134407.3:c.4135A>C MANE Select	NP_001127879.1:p.Ile1379Leu
NM_000833.5:c.4135A>C	NP_000824.1:p.Ile1379Leu