Canonical Allele Identifier: CA645372112

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764809_9764811del , CM000678.2:g.9764809_9764811del	GRCh38
NC_000016.9:g.9858666_9858668del , CM000678.1:g.9858666_9858668del	GRCh37
NC_000016.8:g.9766167_9766169del	NCBI36
NG_011812.1:g.422947_422949del
NG_011812.2:g.422947_422949del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2736_2738del MANE Select	ENSP00000332549.3:p.Ser913del
ENST00000535259.6:c.2265_2267del	ENSP00000441572.3:p.Ser756del
ENST00000636273.2:n.2329_2331del
ENST00000674742.1:c.2265_2267del	ENSP00000502200.1:p.Ser756del
ENST00000675398.1:c.*106_*108del	ENSP00000502752.1:n.*106_*108del
ENST00000330684.3:c.2736_2738del	ENSP00000332549.3:p.Ser913del
ENST00000396573.6:c.2736_2738del	ENSP00000379818.2:p.Ser913del
ENST00000396575.6:c.2325_2327del	ENSP00000379820.3:p.Ser776del
ENST00000461292.3:n.2375_2377del
ENST00000535259.5:c.2325_2327del	ENSP00000441572.2:p.Ser776del
ENST00000562109.5:c.2736_2738del	ENSP00000454998.1:p.Ser913del
NM_000833.4:c.2736_2738del	NP_000824.1:p.Ser913del
NM_001134407.2:c.2736_2738del	NP_001127879.1:p.Ser913del
NM_001134408.2:c.2736_2738del	NP_001127880.1:p.Ser913del
XM_011522456.1:c.2577_2579del	XP_011520758.1:p.Ser860del
XM_011522457.1:c.2478_2480del	XP_011520759.1:p.Ser827del
XM_011522458.1:c.2265_2267del	XP_011520760.1:p.Ser756del
XM_011522459.1:c.2265_2267del	XP_011520761.1:p.Ser756del
XM_011522460.1:c.2265_2267del	XP_011520762.1:p.Ser756del
XM_011522461.1:c.2736_2738del	XP_011520763.1:p.Ser913del
XM_011522458.3:c.2265_2267del	XP_011520760.1:p.Ser756del
XM_011522461.3:c.2736_2738del	XP_011520763.1:p.Ser913del
XM_017023172.1:c.2892_2894del	XP_016878661.1:p.Ser965del
XM_017023173.1:c.2892_2894del	XP_016878662.1:p.Ser965del
NM_001134407.3:c.2736_2738del MANE Select	NP_001127879.1:p.Ser913del
NM_000833.5:c.2736_2738del	NP_000824.1:p.Ser913del