Canonical Allele Identifier: CA2590992970

Gene: GRIN2A

Linked Data

• gnomAD v3: 16-9764704-C-CTGT
• gnomAD v4: 16-9764704-C-CTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764708_9764710dup , CM000678.2:g.9764708_9764710dup	GRCh38
NC_000016.9:g.9858565_9858567dup , CM000678.1:g.9858565_9858567dup	GRCh37
NC_000016.8:g.9766066_9766068dup	NCBI36
NG_011812.1:g.423048_423050dup
NG_011812.2:g.423048_423050dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2837_2839dup MANE Select	ENSP00000332549.3:p.Asn946_Arg947insAsn
ENST00000535259.6:c.2366_2368dup	ENSP00000441572.3:p.Asn789_Arg790insAsn
ENST00000636273.2:n.2430_2432dup
ENST00000674742.1:c.2366_2368dup	ENSP00000502200.1:p.Asn789_Arg790insAsn
ENST00000675398.1:c.*207_*209dup	ENSP00000502752.1:n.*207_*209dup
ENST00000330684.3:c.2837_2839dup	ENSP00000332549.3:p.Asn946_Arg947insAsn
ENST00000396573.6:c.2837_2839dup	ENSP00000379818.2:p.Asn946_Arg947insAsn
ENST00000396575.6:c.2426_2428dup	ENSP00000379820.3:p.Asn809_Arg810insAsn
ENST00000461292.3:n.2476_2478dup
ENST00000535259.5:c.2426_2428dup	ENSP00000441572.2:p.Asn809_Arg810insAsn
ENST00000562109.5:c.2837_2839dup	ENSP00000454998.1:p.Asn946_Arg947insAsn
NM_000833.4:c.2837_2839dup	NP_000824.1:p.Asn946_Arg947insAsn
NM_001134407.2:c.2837_2839dup	NP_001127879.1:p.Asn946_Arg947insAsn
NM_001134408.2:c.2837_2839dup	NP_001127880.1:p.Asn946_Arg947insAsn
XM_011522456.1:c.2678_2680dup	XP_011520758.1:p.Asn893_Arg894insAsn
XM_011522457.1:c.2579_2581dup	XP_011520759.1:p.Asn860_Arg861insAsn
XM_011522458.1:c.2366_2368dup	XP_011520760.1:p.Asn789_Arg790insAsn
XM_011522459.1:c.2366_2368dup	XP_011520761.1:p.Asn789_Arg790insAsn
XM_011522460.1:c.2366_2368dup	XP_011520762.1:p.Asn789_Arg790insAsn
XM_011522461.1:c.2837_2839dup	XP_011520763.1:p.Asn946_Arg947insAsn
XM_011522458.3:c.2366_2368dup	XP_011520760.1:p.Asn789_Arg790insAsn
XM_011522461.3:c.2837_2839dup	XP_011520763.1:p.Asn946_Arg947insAsn
XM_017023172.1:c.2993_2995dup	XP_016878661.1:p.Asn998_Arg999insAsn
XM_017023173.1:c.2993_2995dup	XP_016878662.1:p.Asn998_Arg999insAsn
NM_001134407.3:c.2837_2839dup MANE Select	NP_001127879.1:p.Asn946_Arg947insAsn
NM_000833.5:c.2837_2839dup	NP_000824.1:p.Asn946_Arg947insAsn