Canonical Allele Identifier: CA7896441

Gene: GRIN2A

Linked Data

• ClinVar Variation Id: 2016521
• ClinVar RCV Id: RCV002843941
• dbSNP Id: rs764394577
• ExAC: 16:9858731 G / A
• gnomAD v2: 16-9858731-G-A
• gnomAD v4: 16-9764874-G-A
• COSMIC: COSM5608983
• MyVariant Identifiers: chr16:g.9858731G>A (hg19) ; chr16:g.9764874G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764874G>A , CM000678.2:g.9764874G>A	GRCh38
NC_000016.9:g.9858731G>A , CM000678.1:g.9858731G>A	GRCh37
NC_000016.8:g.9766232G>A	NCBI36
NG_011812.1:g.422881C>T
NG_011812.2:g.422881C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2670C>T MANE Select	ENSP00000332549.3:p.Ser890=
ENST00000535259.6:c.2199C>T	ENSP00000441572.3:p.Ser733=
ENST00000636273.2:n.2263C>T
ENST00000674742.1:c.2199C>T	ENSP00000502200.1:p.Ser733=
ENST00000675398.1:c.*40C>T	ENSP00000502752.1:n.*40C>T
ENST00000330684.3:c.2670C>T	ENSP00000332549.3:p.Ser890=
ENST00000396573.6:c.2670C>T	ENSP00000379818.2:p.Ser890=
ENST00000396575.6:c.2259C>T	ENSP00000379820.3:p.Ser753=
ENST00000461292.3:n.2309C>T
ENST00000463531.1:n.453C>T
ENST00000535259.5:c.2259C>T	ENSP00000441572.2:p.Ser753=
ENST00000562109.5:c.2670C>T	ENSP00000454998.1:p.Ser890=
NM_000833.4:c.2670C>T	NP_000824.1:p.Ser890=
NM_001134407.2:c.2670C>T	NP_001127879.1:p.Ser890=
NM_001134408.2:c.2670C>T	NP_001127880.1:p.Ser890=
XM_011522456.1:c.2511C>T	XP_011520758.1:p.Ser837=
XM_011522457.1:c.2412C>T	XP_011520759.1:p.Ser804=
XM_011522458.1:c.2199C>T	XP_011520760.1:p.Ser733=
XM_011522459.1:c.2199C>T	XP_011520761.1:p.Ser733=
XM_011522460.1:c.2199C>T	XP_011520762.1:p.Ser733=
XM_011522461.1:c.2670C>T	XP_011520763.1:p.Ser890=
XM_011522458.3:c.2199C>T	XP_011520760.1:p.Ser733=
XM_011522461.3:c.2670C>T	XP_011520763.1:p.Ser890=
XM_017023172.1:c.2826C>T	XP_016878661.1:p.Ser942=
XM_017023173.1:c.2826C>T	XP_016878662.1:p.Ser942=
NM_001134407.3:c.2670C>T MANE Select	NP_001127879.1:p.Ser890=
NM_000833.5:c.2670C>T	NP_000824.1:p.Ser890=