Canonical Allele Identifier: CA394798022

Gene: GRIN2A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9937958C>A , CM000678.2:g.9937958C>A	GRCh38
NC_000016.9:g.10031815C>A , CM000678.1:g.10031815C>A	GRCh37
NC_000016.8:g.9939316C>A	NCBI36
NG_011812.1:g.249797G>T
NG_011812.2:g.249797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1007+1G>T MANE Select	ENSP00000332549.3:n.1007+1G>T
ENST00000535259.6:c.536+1G>T	ENSP00000441572.3:n.536+1G>T
ENST00000636273.2:n.600+1G>T
ENST00000637393.1:c.600G>T	ENSP00000490232.1:p.Pro200=
ENST00000674742.1:c.536+1G>T	ENSP00000502200.1:n.536+1G>T
ENST00000675189.1:n.1491+1G>T
ENST00000675398.1:c.1007+1G>T	ENSP00000502752.1:n.1007+1G>T
ENST00000330684.3:c.1007+1G>T	ENSP00000332549.3:n.1007+1G>T
ENST00000396573.6:c.1007+1G>T	ENSP00000379818.2:n.1007+1G>T
ENST00000396575.6:c.596+1G>T	ENSP00000379820.3:n.596+1G>T
ENST00000461292.3:n.646+1G>T
ENST00000535259.5:c.596+1G>T	ENSP00000441572.2:n.596+1G>T
ENST00000562109.5:c.1007+1G>T	ENSP00000454998.1:n.1007+1G>T
ENST00000566683.1:n.241-46858G>T
ENST00000568247.3:n.900G>T
NM_000833.4:c.1007+1G>T	NP_000824.1:n.1007+1G>T
NM_001134407.2:c.1007+1G>T	NP_001127879.1:n.1007+1G>T
NM_001134408.2:c.1007+1G>T	NP_001127880.1:n.1007+1G>T
XM_011522456.1:c.848+1G>T	XP_011520758.1:n.848+1G>T
XM_011522457.1:c.749+1G>T	XP_011520759.1:n.749+1G>T
XM_011522458.1:c.536+1G>T	XP_011520760.1:n.536+1G>T
XM_011522459.1:c.536+1G>T	XP_011520761.1:n.536+1G>T
XM_011522460.1:c.536+1G>T	XP_011520762.1:n.536+1G>T
XM_011522461.1:c.1007+1G>T	XP_011520763.1:n.1007+1G>T
XM_011522458.3:c.536+1G>T	XP_011520760.1:n.536+1G>T
XM_011522461.3:c.1007+1G>T	XP_011520763.1:n.1007+1G>T
XM_017023172.1:c.1163+1G>T	XP_016878661.1:n.1163+1G>T
XM_017023173.1:c.1163+1G>T	XP_016878662.1:n.1163+1G>T
NM_001134407.3:c.1007+1G>T MANE Select	NP_001127879.1:n.1007+1G>T
NM_000833.5:c.1007+1G>T	NP_000824.1:n.1007+1G>T