Canonical Allele Identifier: CA394705922

Gene: GRIN2A

Linked Data

• COSMIC: COSM5696043
• MyVariant Identifiers: chr16:g.9857233A>C (hg19) ; chr16:g.9763376A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763376A>C , CM000678.2:g.9763376A>C	GRCh38
NC_000016.9:g.9857233A>C , CM000678.1:g.9857233A>C	GRCh37
NC_000016.8:g.9764734A>C	NCBI36
NG_011812.1:g.424379T>G
NG_011812.2:g.424379T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4168T>G MANE Select	ENSP00000332549.3:p.Ser1390Ala
ENST00000535259.6:c.3354T>G	ENSP00000441572.3:p.Thr1118=
ENST00000636273.2:n.3418T>G
ENST00000674742.1:c.3697T>G	ENSP00000502200.1:p.Ser1233Ala
ENST00000675398.1:c.*1538T>G	ENSP00000502752.1:n.*1538T>G
ENST00000330684.3:c.4168T>G	ENSP00000332549.3:p.Ser1390Ala
ENST00000396573.6:c.4168T>G	ENSP00000379818.2:p.Ser1390Ala
ENST00000396575.6:c.3757T>G	ENSP00000379820.3:p.Ser1253Ala
ENST00000461292.3:n.3464T>G
ENST00000535259.5:c.3414T>G	ENSP00000441572.2:p.Thr1138=
ENST00000562109.5:c.3825T>G	ENSP00000454998.1:p.Thr1275=
NM_000833.4:c.4168T>G	NP_000824.1:p.Ser1390Ala
NM_001134407.2:c.4168T>G	NP_001127879.1:p.Ser1390Ala
NM_001134408.2:c.3825T>G	NP_001127880.1:p.Thr1275=
XM_011522456.1:c.4009T>G	XP_011520758.1:p.Ser1337Ala
XM_011522457.1:c.3910T>G	XP_011520759.1:p.Ser1304Ala
XM_011522458.1:c.3697T>G	XP_011520760.1:p.Ser1233Ala
XM_011522459.1:c.3697T>G	XP_011520761.1:p.Ser1233Ala
XM_011522460.1:c.3697T>G	XP_011520762.1:p.Ser1233Ala
XM_011522461.1:c.3825T>G	XP_011520763.1:p.Thr1275=
XM_011522458.3:c.3697T>G	XP_011520760.1:p.Ser1233Ala
XM_011522461.3:c.3825T>G	XP_011520763.1:p.Thr1275=
XM_017023172.1:c.4324T>G	XP_016878661.1:p.Ser1442Ala
XM_017023173.1:c.3981T>G	XP_016878662.1:p.Thr1327=
NM_001134407.3:c.4168T>G MANE Select	NP_001127879.1:p.Ser1390Ala
NM_000833.5:c.4168T>G	NP_000824.1:p.Ser1390Ala