Canonical Allele Identifier: CA314949

Gene: GRIN2A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9798436C>T , CM000678.2:g.9798436C>T	GRCh38
NC_000016.9:g.9892293C>T , CM000678.1:g.9892293C>T	GRCh37
NC_000016.8:g.9799794C>T	NCBI36
NG_011812.1:g.389319G>A
NG_011812.2:g.389319G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2197G>A MANE Select	ENSP00000332549.3:p.Ala733Thr
ENST00000535259.6:c.1726G>A	ENSP00000441572.3:p.Ala576Thr
ENST00000636273.2:n.1790G>A
ENST00000674742.1:c.1726G>A	ENSP00000502200.1:p.Ala576Thr
ENST00000675398.1:c.2197G>A	ENSP00000502752.1:p.Ala733Thr
ENST00000330684.3:c.2197G>A	ENSP00000332549.3:p.Ala733Thr
ENST00000396573.6:c.2197G>A	ENSP00000379818.2:p.Ala733Thr
ENST00000396575.6:c.1786G>A	ENSP00000379820.3:p.Ala596Thr
ENST00000461292.3:n.1836G>A
ENST00000535259.5:c.1786G>A	ENSP00000441572.2:p.Ala596Thr
ENST00000562109.5:c.2197G>A	ENSP00000454998.1:p.Ala733Thr
NM_000833.4:c.2197G>A	NP_000824.1:p.Ala733Thr
NM_001134407.2:c.2197G>A	NP_001127879.1:p.Ala733Thr
NM_001134408.2:c.2197G>A	NP_001127880.1:p.Ala733Thr
XM_011522456.1:c.2038G>A	XP_011520758.1:p.Ala680Thr
XM_011522457.1:c.1939G>A	XP_011520759.1:p.Ala647Thr
XM_011522458.1:c.1726G>A	XP_011520760.1:p.Ala576Thr
XM_011522459.1:c.1726G>A	XP_011520761.1:p.Ala576Thr
XM_011522460.1:c.1726G>A	XP_011520762.1:p.Ala576Thr
XM_011522461.1:c.2197G>A	XP_011520763.1:p.Ala733Thr
XR_933062.1:n.300+3714C>T
XR_933063.1:n.300+3714C>T
XM_011522458.3:c.1726G>A	XP_011520760.1:p.Ala576Thr
XM_011522461.3:c.2197G>A	XP_011520763.1:p.Ala733Thr
XM_017023172.1:c.2353G>A	XP_016878661.1:p.Ala785Thr
XM_017023173.1:c.2353G>A	XP_016878662.1:p.Ala785Thr
XR_933062.3:n.3304+3714C>T
XR_933063.3:n.3304+3714C>T
NM_001134407.3:c.2197G>A MANE Select	NP_001127879.1:p.Ala733Thr
NM_000833.5:c.2197G>A	NP_000824.1:p.Ala733Thr