Canonical Allele Identifier: CA394706089

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1567275428
• MyVariant Identifiers: chr16:g.9857296G>A (hg19) ; chr16:g.9763439G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763439G>A , CM000678.2:g.9763439G>A	GRCh38
NC_000016.9:g.9857296G>A , CM000678.1:g.9857296G>A	GRCh37
NC_000016.8:g.9764797G>A	NCBI36
NG_011812.1:g.424316C>T
NG_011812.2:g.424316C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4105C>T MANE Select	ENSP00000332549.3:p.His1369Tyr
ENST00000535259.6:c.3302-11C>T	ENSP00000441572.3:n.3302-11C>T
ENST00000636273.2:n.3366-11C>T
ENST00000674742.1:c.3634C>T	ENSP00000502200.1:p.His1212Tyr
ENST00000675398.1:c.*1475C>T	ENSP00000502752.1:n.*1475C>T
ENST00000330684.3:c.4105C>T	ENSP00000332549.3:p.His1369Tyr
ENST00000396573.6:c.4105C>T	ENSP00000379818.2:p.His1369Tyr
ENST00000396575.6:c.3694C>T	ENSP00000379820.3:p.His1232Tyr
ENST00000461292.3:n.3412-11C>T
ENST00000535259.5:c.3362-11C>T	ENSP00000441572.2:n.3362-11C>T
ENST00000562109.5:c.3773-11C>T	ENSP00000454998.1:n.3773-11C>T
NM_000833.4:c.4105C>T	NP_000824.1:p.His1369Tyr
NM_001134407.2:c.4105C>T	NP_001127879.1:p.His1369Tyr
NM_001134408.2:c.3773-11C>T	NP_001127880.1:n.3773-11C>T
XM_011522456.1:c.3946C>T	XP_011520758.1:p.His1316Tyr
XM_011522457.1:c.3847C>T	XP_011520759.1:p.His1283Tyr
XM_011522458.1:c.3634C>T	XP_011520760.1:p.His1212Tyr
XM_011522459.1:c.3634C>T	XP_011520761.1:p.His1212Tyr
XM_011522460.1:c.3634C>T	XP_011520762.1:p.His1212Tyr
XM_011522461.1:c.3773-11C>T	XP_011520763.1:n.3773-11C>T
XM_011522458.3:c.3634C>T	XP_011520760.1:p.His1212Tyr
XM_011522461.3:c.3773-11C>T	XP_011520763.1:n.3773-11C>T
XM_017023172.1:c.4261C>T	XP_016878661.1:p.His1421Tyr
XM_017023173.1:c.3929-11C>T	XP_016878662.1:n.3929-11C>T
NM_001134407.3:c.4105C>T MANE Select	NP_001127879.1:p.His1369Tyr
NM_000833.5:c.4105C>T	NP_000824.1:p.His1369Tyr