Canonical Allele Identifier: CA493692780

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 2103337
• ClinVar RCV Id: RCV003028832
• dbSNP Id: rs1167057636
• gnomAD v2: 16-9857375-G-A
• gnomAD v4: 16-9763518-G-A
• MyVariant Identifiers: chr16:g.9857375G>A (hg19) ; chr16:g.9763518G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763518G>A , CM000678.2:g.9763518G>A	GRCh38
NC_000016.9:g.9857375G>A , CM000678.1:g.9857375G>A	GRCh37
NC_000016.8:g.9764876G>A	NCBI36
NG_011812.1:g.424237C>T
NG_011812.2:g.424237C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4026C>T MANE Select	ENSP00000332549.3:p.Ser1342=
ENST00000535259.6:c.3302-90C>T	ENSP00000441572.3:n.3302-90C>T
ENST00000636273.2:n.3366-90C>T
ENST00000674742.1:c.3555C>T	ENSP00000502200.1:p.Ser1185=
ENST00000675398.1:c.*1396C>T	ENSP00000502752.1:n.*1396C>T
ENST00000330684.3:c.4026C>T	ENSP00000332549.3:p.Ser1342=
ENST00000396573.6:c.4026C>T	ENSP00000379818.2:p.Ser1342=
ENST00000396575.6:c.3615C>T	ENSP00000379820.3:p.Ser1205=
ENST00000461292.3:n.3412-90C>T
ENST00000535259.5:c.3362-90C>T	ENSP00000441572.2:n.3362-90C>T
ENST00000562109.5:c.3773-90C>T	ENSP00000454998.1:n.3773-90C>T
NM_000833.4:c.4026C>T	NP_000824.1:p.Ser1342=
NM_001134407.2:c.4026C>T	NP_001127879.1:p.Ser1342=
NM_001134408.2:c.3773-90C>T	NP_001127880.1:n.3773-90C>T
XM_011522456.1:c.3867C>T	XP_011520758.1:p.Ser1289=
XM_011522457.1:c.3768C>T	XP_011520759.1:p.Ser1256=
XM_011522458.1:c.3555C>T	XP_011520760.1:p.Ser1185=
XM_011522459.1:c.3555C>T	XP_011520761.1:p.Ser1185=
XM_011522460.1:c.3555C>T	XP_011520762.1:p.Ser1185=
XM_011522461.1:c.3773-90C>T	XP_011520763.1:n.3773-90C>T
XM_011522458.3:c.3555C>T	XP_011520760.1:p.Ser1185=
XM_011522461.3:c.3773-90C>T	XP_011520763.1:n.3773-90C>T
XM_017023172.1:c.4182C>T	XP_016878661.1:p.Ser1394=
XM_017023173.1:c.3929-90C>T	XP_016878662.1:n.3929-90C>T
NM_001134407.3:c.4026C>T MANE Select	NP_001127879.1:p.Ser1342=
NM_000833.5:c.4026C>T	NP_000824.1:p.Ser1342=