Canonical Allele Identifier: CA14324352

Gene: GRIN2A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10089230T>C , CM000678.2:g.10089230T>C	GRCh38
NC_000016.9:g.10183087T>C , CM000678.1:g.10183087T>C	GRCh37
NC_000016.8:g.10090588T>C	NCBI36
NG_011812.1:g.98525A>G
NG_011812.2:g.98525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.414+90768A>G MANE Select	ENSP00000332549.3:n.414+90768A>G
ENST00000637393.1:c.6+90768A>G	ENSP00000490232.1:n.6+90768A>G
ENST00000674742.1:c.-58+32098A>G	ENSP00000502200.1:n.-58+32098A>G
ENST00000675189.1:n.898+90768A>G
ENST00000675398.1:c.414+90768A>G	ENSP00000502752.1:n.414+90768A>G
ENST00000330684.3:c.414+90768A>G	ENSP00000332549.3:n.414+90768A>G
ENST00000396573.6:c.414+90768A>G	ENSP00000379818.2:n.414+90768A>G
ENST00000562109.5:c.414+90768A>G	ENSP00000454998.1:n.414+90768A>G
NM_000833.4:c.414+90768A>G	NP_000824.1:n.414+90768A>G
NM_001134407.2:c.414+90768A>G	NP_001127879.1:n.414+90768A>G
NM_001134408.2:c.414+90768A>G	NP_001127880.1:n.414+90768A>G
XM_011522461.1:c.414+90768A>G	XP_011520763.1:n.414+90768A>G
XM_011522461.3:c.414+90768A>G	XP_011520763.1:n.414+90768A>G
XM_017023172.1:c.570+90768A>G	XP_016878661.1:n.570+90768A>G
XM_017023173.1:c.570+90768A>G	XP_016878662.1:n.570+90768A>G
NM_001134407.3:c.414+90768A>G MANE Select	NP_001127879.1:n.414+90768A>G
NM_000833.5:c.414+90768A>G	NP_000824.1:n.414+90768A>G