Canonical Allele Identifier: CA493702305

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10032217A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938360A>G , CM000678.2:g.9938360A>G	GRCh38
NC_000016.9:g.10032217A>G , CM000678.1:g.10032217A>G	GRCh37
NC_000016.8:g.9939718A>G	NCBI36
NG_011812.1:g.249395T>C
NG_011812.2:g.249395T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.606T>C MANE Select	ENSP00000332549.3:p.Asn202=
ENST00000535259.6:c.135T>C	ENSP00000441572.3:p.Asn45=
ENST00000636273.2:n.199T>C
ENST00000637393.1:c.198T>C	ENSP00000490232.1:p.Asn66=
ENST00000674742.1:c.135T>C	ENSP00000502200.1:p.Asn45=
ENST00000675189.1:n.1090T>C
ENST00000675398.1:c.606T>C	ENSP00000502752.1:p.Asn202=
ENST00000330684.3:c.606T>C	ENSP00000332549.3:p.Asn202=
ENST00000396573.6:c.606T>C	ENSP00000379818.2:p.Asn202=
ENST00000396575.6:c.195T>C	ENSP00000379820.3:p.Asn65=
ENST00000461292.3:n.245T>C
ENST00000535259.5:c.195T>C	ENSP00000441572.2:p.Asn65=
ENST00000562109.5:c.606T>C	ENSP00000454998.1:p.Asn202=
ENST00000566670.2:n.448T>C
ENST00000566683.1:n.241-47260T>C
ENST00000568247.3:n.498T>C
NM_000833.4:c.606T>C	NP_000824.1:p.Asn202=
NM_001134407.2:c.606T>C	NP_001127879.1:p.Asn202=
NM_001134408.2:c.606T>C	NP_001127880.1:p.Asn202=
XM_011522456.1:c.447T>C	XP_011520758.1:p.Asn149=
XM_011522457.1:c.348T>C	XP_011520759.1:p.Asn116=
XM_011522458.1:c.135T>C	XP_011520760.1:p.Asn45=
XM_011522459.1:c.135T>C	XP_011520761.1:p.Asn45=
XM_011522460.1:c.135T>C	XP_011520762.1:p.Asn45=
XM_011522461.1:c.606T>C	XP_011520763.1:p.Asn202=
XM_011522458.3:c.135T>C	XP_011520760.1:p.Asn45=
XM_011522461.3:c.606T>C	XP_011520763.1:p.Asn202=
XM_017023172.1:c.762T>C	XP_016878661.1:p.Asn254=
XM_017023173.1:c.762T>C	XP_016878662.1:p.Asn254=
NM_001134407.3:c.606T>C MANE Select	NP_001127879.1:p.Asn202=
NM_000833.5:c.606T>C	NP_000824.1:p.Asn202=