Canonical Allele Identifier: CA493683130

Gene: GRIN2A

Linked Data

• MyVariant Identifiers: chr16:g.10031917A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938060A>C , CM000678.2:g.9938060A>C	GRCh38
NC_000016.9:g.10031917A>C , CM000678.1:g.10031917A>C	GRCh37
NC_000016.8:g.9939418A>C	NCBI36
NG_011812.1:g.249695T>G
NG_011812.2:g.249695T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.906T>G MANE Select	ENSP00000332549.3:p.Ala302=
ENST00000535259.6:c.435T>G	ENSP00000441572.3:p.Ala145=
ENST00000636273.2:n.499T>G
ENST00000637393.1:c.498T>G	ENSP00000490232.1:p.Ala166=
ENST00000674742.1:c.435T>G	ENSP00000502200.1:p.Ala145=
ENST00000675189.1:n.1390T>G
ENST00000675398.1:c.906T>G	ENSP00000502752.1:p.Ala302=
ENST00000330684.3:c.906T>G	ENSP00000332549.3:p.Ala302=
ENST00000396573.6:c.906T>G	ENSP00000379818.2:p.Ala302=
ENST00000396575.6:c.495T>G	ENSP00000379820.3:p.Ala165=
ENST00000461292.3:n.545T>G
ENST00000535259.5:c.495T>G	ENSP00000441572.2:p.Ala165=
ENST00000562109.5:c.906T>G	ENSP00000454998.1:p.Ala302=
ENST00000566683.1:n.241-46960T>G
ENST00000568247.3:n.798T>G
NM_000833.4:c.906T>G	NP_000824.1:p.Ala302=
NM_001134407.2:c.906T>G	NP_001127879.1:p.Ala302=
NM_001134408.2:c.906T>G	NP_001127880.1:p.Ala302=
XM_011522456.1:c.747T>G	XP_011520758.1:p.Ala249=
XM_011522457.1:c.648T>G	XP_011520759.1:p.Ala216=
XM_011522458.1:c.435T>G	XP_011520760.1:p.Ala145=
XM_011522459.1:c.435T>G	XP_011520761.1:p.Ala145=
XM_011522460.1:c.435T>G	XP_011520762.1:p.Ala145=
XM_011522461.1:c.906T>G	XP_011520763.1:p.Ala302=
XM_011522458.3:c.435T>G	XP_011520760.1:p.Ala145=
XM_011522461.3:c.906T>G	XP_011520763.1:p.Ala302=
XM_017023172.1:c.1062T>G	XP_016878661.1:p.Ala354=
XM_017023173.1:c.1062T>G	XP_016878662.1:p.Ala354=
NM_001134407.3:c.906T>G MANE Select	NP_001127879.1:p.Ala302=
NM_000833.5:c.906T>G	NP_000824.1:p.Ala302=