Canonical Allele Identifier: CA645570179

Gene: GRIN2A

Linked Data

• COSMIC: COSM5943150

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763619_9763620insA , CM000678.2:g.9763619_9763620insA	GRCh38
NC_000016.9:g.9857476_9857477insA , CM000678.1:g.9857476_9857477insA	GRCh37
NC_000016.8:g.9764977_9764978insA	NCBI36
NG_011812.1:g.424135_424136insT
NG_011812.2:g.424135_424136insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3924_3925insT MANE Select	ENSP00000332549.3:p.Arg1309SerfsTer22
ENST00000535259.6:c.3301+152_3301+153insT	ENSP00000441572.3:n.3301+152_3301+153insT
ENST00000636273.2:n.3365+152_3365+153insT
ENST00000674742.1:c.3453_3454insT	ENSP00000502200.1:p.Arg1152SerfsTer22
ENST00000675398.1:c.*1294_*1295insT	ENSP00000502752.1:n.*1294_*1295insT
ENST00000330684.3:c.3924_3925insT	ENSP00000332549.3:p.Arg1309SerfsTer22
ENST00000396573.6:c.3924_3925insT	ENSP00000379818.2:p.Arg1309SerfsTer22
ENST00000396575.6:c.3513_3514insT	ENSP00000379820.3:p.Arg1172SerfsTer22
ENST00000461292.3:n.3411+152_3411+153insT
ENST00000535259.5:c.3361+152_3361+153insT	ENSP00000441572.2:n.3361+152_3361+153insT
ENST00000562109.5:c.3772+152_3772+153insT	ENSP00000454998.1:n.3772+152_3772+153insT
NM_000833.4:c.3924_3925insT	NP_000824.1:p.Arg1309SerfsTer22
NM_001134407.2:c.3924_3925insT	NP_001127879.1:p.Arg1309SerfsTer22
NM_001134408.2:c.3772+152_3772+153insT	NP_001127880.1:n.3772+152_3772+153insT
XM_011522456.1:c.3765_3766insT	XP_011520758.1:p.Arg1256SerfsTer22
XM_011522457.1:c.3666_3667insT	XP_011520759.1:p.Arg1223SerfsTer22
XM_011522458.1:c.3453_3454insT	XP_011520760.1:p.Arg1152SerfsTer22
XM_011522459.1:c.3453_3454insT	XP_011520761.1:p.Arg1152SerfsTer22
XM_011522460.1:c.3453_3454insT	XP_011520762.1:p.Arg1152SerfsTer22
XM_011522461.1:c.3772+152_3772+153insT	XP_011520763.1:n.3772+152_3772+153insT
XM_011522458.3:c.3453_3454insT	XP_011520760.1:p.Arg1152SerfsTer22
XM_011522461.3:c.3772+152_3772+153insT	XP_011520763.1:n.3772+152_3772+153insT
XM_017023172.1:c.4080_4081insT	XP_016878661.1:p.Arg1361SerfsTer22
XM_017023173.1:c.3928+152_3928+153insT	XP_016878662.1:n.3928+152_3928+153insT
NM_001134407.3:c.3924_3925insT MANE Select	NP_001127879.1:p.Arg1309SerfsTer22
NM_000833.5:c.3924_3925insT	NP_000824.1:p.Arg1309SerfsTer22