Canonical Allele Identifier: CA394706435

Gene: GRIN2A

Linked Data

• dbSNP Id: rs1036750557
• MyVariant Identifiers: chr16:g.9857424C>A (hg19) ; chr16:g.9763567C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763567C>A , CM000678.2:g.9763567C>A	GRCh38
NC_000016.9:g.9857424C>A , CM000678.1:g.9857424C>A	GRCh37
NC_000016.8:g.9764925C>A	NCBI36
NG_011812.1:g.424188G>T
NG_011812.2:g.424188G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3977G>T MANE Select	ENSP00000332549.3:p.Gly1326Val
ENST00000535259.6:c.3302-139G>T	ENSP00000441572.3:n.3302-139G>T
ENST00000636273.2:n.3366-139G>T
ENST00000674742.1:c.3506G>T	ENSP00000502200.1:p.Gly1169Val
ENST00000675398.1:c.*1347G>T	ENSP00000502752.1:n.*1347G>T
ENST00000330684.3:c.3977G>T	ENSP00000332549.3:p.Gly1326Val
ENST00000396573.6:c.3977G>T	ENSP00000379818.2:p.Gly1326Val
ENST00000396575.6:c.3566G>T	ENSP00000379820.3:p.Gly1189Val
ENST00000461292.3:n.3412-139G>T
ENST00000535259.5:c.3362-139G>T	ENSP00000441572.2:n.3362-139G>T
ENST00000562109.5:c.3773-139G>T	ENSP00000454998.1:n.3773-139G>T
NM_000833.4:c.3977G>T	NP_000824.1:p.Gly1326Val
NM_001134407.2:c.3977G>T	NP_001127879.1:p.Gly1326Val
NM_001134408.2:c.3773-139G>T	NP_001127880.1:n.3773-139G>T
XM_011522456.1:c.3818G>T	XP_011520758.1:p.Gly1273Val
XM_011522457.1:c.3719G>T	XP_011520759.1:p.Gly1240Val
XM_011522458.1:c.3506G>T	XP_011520760.1:p.Gly1169Val
XM_011522459.1:c.3506G>T	XP_011520761.1:p.Gly1169Val
XM_011522460.1:c.3506G>T	XP_011520762.1:p.Gly1169Val
XM_011522461.1:c.3773-139G>T	XP_011520763.1:n.3773-139G>T
XM_011522458.3:c.3506G>T	XP_011520760.1:p.Gly1169Val
XM_011522461.3:c.3773-139G>T	XP_011520763.1:n.3773-139G>T
XM_017023172.1:c.4133G>T	XP_016878661.1:p.Gly1378Val
XM_017023173.1:c.3929-139G>T	XP_016878662.1:n.3929-139G>T
NM_001134407.3:c.3977G>T MANE Select	NP_001127879.1:p.Gly1326Val
NM_000833.5:c.3977G>T	NP_000824.1:p.Gly1326Val