Canonical Allele Identifier: CA394705958

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141126067
• MyVariant Identifiers: chr16:g.9857245G>C (hg19) ; chr16:g.9763388G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763388G>C , CM000678.2:g.9763388G>C	GRCh38
NC_000016.9:g.9857245G>C , CM000678.1:g.9857245G>C	GRCh37
NC_000016.8:g.9764746G>C	NCBI36
NG_011812.1:g.424367C>G
NG_011812.2:g.424367C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4156C>G MANE Select	ENSP00000332549.3:p.Pro1386Ala
ENST00000535259.6:c.3342C>G	ENSP00000441572.3:p.Thr1114=
ENST00000636273.2:n.3406C>G
ENST00000674742.1:c.3685C>G	ENSP00000502200.1:p.Pro1229Ala
ENST00000675398.1:c.*1526C>G	ENSP00000502752.1:n.*1526C>G
ENST00000330684.3:c.4156C>G	ENSP00000332549.3:p.Pro1386Ala
ENST00000396573.6:c.4156C>G	ENSP00000379818.2:p.Pro1386Ala
ENST00000396575.6:c.3745C>G	ENSP00000379820.3:p.Pro1249Ala
ENST00000461292.3:n.3452C>G
ENST00000535259.5:c.3402C>G	ENSP00000441572.2:p.Thr1134=
ENST00000562109.5:c.3813C>G	ENSP00000454998.1:p.Thr1271=
NM_000833.4:c.4156C>G	NP_000824.1:p.Pro1386Ala
NM_001134407.2:c.4156C>G	NP_001127879.1:p.Pro1386Ala
NM_001134408.2:c.3813C>G	NP_001127880.1:p.Thr1271=
XM_011522456.1:c.3997C>G	XP_011520758.1:p.Pro1333Ala
XM_011522457.1:c.3898C>G	XP_011520759.1:p.Pro1300Ala
XM_011522458.1:c.3685C>G	XP_011520760.1:p.Pro1229Ala
XM_011522459.1:c.3685C>G	XP_011520761.1:p.Pro1229Ala
XM_011522460.1:c.3685C>G	XP_011520762.1:p.Pro1229Ala
XM_011522461.1:c.3813C>G	XP_011520763.1:p.Thr1271=
XM_011522458.3:c.3685C>G	XP_011520760.1:p.Pro1229Ala
XM_011522461.3:c.3813C>G	XP_011520763.1:p.Thr1271=
XM_017023172.1:c.4312C>G	XP_016878661.1:p.Pro1438Ala
XM_017023173.1:c.3969C>G	XP_016878662.1:p.Thr1323=
NM_001134407.3:c.4156C>G MANE Select	NP_001127879.1:p.Pro1386Ala
NM_000833.5:c.4156C>G	NP_000824.1:p.Pro1386Ala