Canonical Allele Identifier: CA394709475

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 1801079
• ClinVar RCV Id: RCV002462676
• gnomAD v4: 16-9764813-T-A
• MyVariant Identifiers: chr16:g.9858670T>A (hg19) ; chr16:g.9764813T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764813T>A , CM000678.2:g.9764813T>A	GRCh38
NC_000016.9:g.9858670T>A , CM000678.1:g.9858670T>A	GRCh37
NC_000016.8:g.9766171T>A	NCBI36
NG_011812.1:g.422942A>T
NG_011812.2:g.422942A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2731A>T MANE Select	ENSP00000332549.3:p.Asn911Tyr
ENST00000535259.6:c.2260A>T	ENSP00000441572.3:p.Asn754Tyr
ENST00000636273.2:n.2324A>T
ENST00000674742.1:c.2260A>T	ENSP00000502200.1:p.Asn754Tyr
ENST00000675398.1:c.*101A>T	ENSP00000502752.1:n.*101A>T
ENST00000330684.3:c.2731A>T	ENSP00000332549.3:p.Asn911Tyr
ENST00000396573.6:c.2731A>T	ENSP00000379818.2:p.Asn911Tyr
ENST00000396575.6:c.2320A>T	ENSP00000379820.3:p.Asn774Tyr
ENST00000461292.3:n.2370A>T
ENST00000535259.5:c.2320A>T	ENSP00000441572.2:p.Asn774Tyr
ENST00000562109.5:c.2731A>T	ENSP00000454998.1:p.Asn911Tyr
NM_000833.4:c.2731A>T	NP_000824.1:p.Asn911Tyr
NM_001134407.2:c.2731A>T	NP_001127879.1:p.Asn911Tyr
NM_001134408.2:c.2731A>T	NP_001127880.1:p.Asn911Tyr
XM_011522456.1:c.2572A>T	XP_011520758.1:p.Asn858Tyr
XM_011522457.1:c.2473A>T	XP_011520759.1:p.Asn825Tyr
XM_011522458.1:c.2260A>T	XP_011520760.1:p.Asn754Tyr
XM_011522459.1:c.2260A>T	XP_011520761.1:p.Asn754Tyr
XM_011522460.1:c.2260A>T	XP_011520762.1:p.Asn754Tyr
XM_011522461.1:c.2731A>T	XP_011520763.1:p.Asn911Tyr
XM_011522458.3:c.2260A>T	XP_011520760.1:p.Asn754Tyr
XM_011522461.3:c.2731A>T	XP_011520763.1:p.Asn911Tyr
XM_017023172.1:c.2887A>T	XP_016878661.1:p.Asn963Tyr
XM_017023173.1:c.2887A>T	XP_016878662.1:p.Asn963Tyr
NM_001134407.3:c.2731A>T MANE Select	NP_001127879.1:p.Asn911Tyr
NM_000833.5:c.2731A>T	NP_000824.1:p.Asn911Tyr