Canonical Allele Identifier: CA2575908542

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-9840639-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9840645_9840646del , CM000678.2:g.9840645_9840646del	GRCh38
NC_000016.9:g.9934502_9934503del , CM000678.1:g.9934502_9934503del	GRCh37
NC_000016.8:g.9842003_9842004del	NCBI36
NG_011812.1:g.347114_347115del
NG_011812.2:g.347114_347115del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.1651+6_1651+7del MANE Select	ENSP00000332549.3:n.1651+6_1651+7del
ENST00000535259.6:c.1180+6_1180+7del	ENSP00000441572.3:n.1180+6_1180+7del
ENST00000636273.2:n.1244+6_1244+7del
ENST00000674742.1:c.1180+6_1180+7del	ENSP00000502200.1:n.1180+6_1180+7del
ENST00000675189.1:n.2135+6_2135+7del
ENST00000675398.1:c.1651+6_1651+7del	ENSP00000502752.1:n.1651+6_1651+7del
ENST00000330684.3:c.1651+6_1651+7del	ENSP00000332549.3:n.1651+6_1651+7del
ENST00000396573.6:c.1651+6_1651+7del	ENSP00000379818.2:n.1651+6_1651+7del
ENST00000396575.6:c.1240+6_1240+7del	ENSP00000379820.3:n.1240+6_1240+7del
ENST00000461292.3:n.1290+6_1290+7del
ENST00000535259.5:c.1240+6_1240+7del	ENSP00000441572.2:n.1240+6_1240+7del
ENST00000562109.5:c.1651+6_1651+7del	ENSP00000454998.1:n.1651+6_1651+7del
NM_000833.4:c.1651+6_1651+7del	NP_000824.1:n.1651+6_1651+7del
NM_001134407.2:c.1651+6_1651+7del	NP_001127879.1:n.1651+6_1651+7del
NM_001134408.2:c.1651+6_1651+7del	NP_001127880.1:n.1651+6_1651+7del
XM_011522456.1:c.1492+6_1492+7del	XP_011520758.1:n.1492+6_1492+7del
XM_011522457.1:c.1393+6_1393+7del	XP_011520759.1:n.1393+6_1393+7del
XM_011522458.1:c.1180+6_1180+7del	XP_011520760.1:n.1180+6_1180+7del
XM_011522459.1:c.1180+6_1180+7del	XP_011520761.1:n.1180+6_1180+7del
XM_011522460.1:c.1180+6_1180+7del	XP_011520762.1:n.1180+6_1180+7del
XM_011522461.1:c.1651+6_1651+7del	XP_011520763.1:n.1651+6_1651+7del
XM_011522458.3:c.1180+6_1180+7del	XP_011520760.1:n.1180+6_1180+7del
XM_011522461.3:c.1651+6_1651+7del	XP_011520763.1:n.1651+6_1651+7del
XM_017023172.1:c.1807+6_1807+7del	XP_016878661.1:n.1807+6_1807+7del
XM_017023173.1:c.1807+6_1807+7del	XP_016878662.1:n.1807+6_1807+7del
NM_001134407.3:c.1651+6_1651+7del MANE Select	NP_001127879.1:n.1651+6_1651+7del
NM_000833.5:c.1651+6_1651+7del	NP_000824.1:n.1651+6_1651+7del