Canonical Allele Identifier: CA2731686089

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2141126867

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763469del , CM000678.2:g.9763469del	GRCh38
NC_000016.9:g.9857326del , CM000678.1:g.9857326del	GRCh37
NC_000016.8:g.9764827del	NCBI36
NG_011812.1:g.424287del
NG_011812.2:g.424287del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4076del MANE Select	ENSP00000332549.3:p.Pro1359GlnfsTer?
ENST00000535259.6:c.3302-40del	ENSP00000441572.3:n.3302-40del
ENST00000636273.2:n.3366-40del
ENST00000674742.1:c.3605del	ENSP00000502200.1:p.Pro1202GlnfsTer?
ENST00000675398.1:c.*1446del	ENSP00000502752.1:n.*1446del
ENST00000330684.3:c.4076del	ENSP00000332549.3:p.Pro1359GlnfsTer?
ENST00000396573.6:c.4076del	ENSP00000379818.2:p.Pro1359GlnfsTer?
ENST00000396575.6:c.3665del	ENSP00000379820.3:p.Pro1222GlnfsTer?
ENST00000461292.3:n.3412-40del
ENST00000535259.5:c.3362-40del	ENSP00000441572.2:n.3362-40del
ENST00000562109.5:c.3773-40del	ENSP00000454998.1:n.3773-40del
NM_000833.4:c.4076del	NP_000824.1:p.Pro1359GlnfsTer?
NM_001134407.2:c.4076del	NP_001127879.1:p.Pro1359GlnfsTer?
NM_001134408.2:c.3773-40del	NP_001127880.1:n.3773-40del
XM_011522456.1:c.3917del	XP_011520758.1:p.Pro1306GlnfsTer?
XM_011522457.1:c.3818del	XP_011520759.1:p.Pro1273GlnfsTer?
XM_011522458.1:c.3605del	XP_011520760.1:p.Pro1202GlnfsTer?
XM_011522459.1:c.3605del	XP_011520761.1:p.Pro1202GlnfsTer?
XM_011522460.1:c.3605del	XP_011520762.1:p.Pro1202GlnfsTer?
XM_011522461.1:c.3773-40del	XP_011520763.1:n.3773-40del
XM_011522458.3:c.3605del	XP_011520760.1:p.Pro1202GlnfsTer?
XM_011522461.3:c.3773-40del	XP_011520763.1:n.3773-40del
XM_017023172.1:c.4232del	XP_016878661.1:p.Pro1411GlnfsTer?
XM_017023173.1:c.3929-40del	XP_016878662.1:n.3929-40del
NM_001134407.3:c.4076del MANE Select	NP_001127879.1:p.Pro1359GlnfsTer?
NM_000833.5:c.4076del	NP_000824.1:p.Pro1359GlnfsTer?