Canonical Allele Identifier: CA2206692761

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763529_9763530delinsTC , CM000678.2:g.9763529_9763530delinsTC	GRCh38
NC_000016.9:g.9857386_9857387delinsTC , CM000678.1:g.9857386_9857387delinsTC	GRCh37
NC_000016.8:g.9764887_9764888delinsTC	NCBI36
NG_011812.1:g.424225_424226delinsGA
NG_011812.2:g.424225_424226delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4014_4015delinsGA MANE Select	ENSP00000332549.3:p.Gly1338=
ENST00000535259.6:c.3302-102_3302-101delinsGA	ENSP00000441572.3:n.3302-102_3302-101delinsGA
ENST00000636273.2:n.3366-102_3366-101delinsGA
ENST00000674742.1:c.3543_3544delinsGA	ENSP00000502200.1:p.Gly1181=
ENST00000675398.1:c.*1384_*1385delinsGA	ENSP00000502752.1:n.*1384_*1385delinsGA
ENST00000330684.3:c.4014_4015delinsGA	ENSP00000332549.3:p.Gly1338=
ENST00000396573.6:c.4014_4015delinsGA	ENSP00000379818.2:p.Gly1338=
ENST00000396575.6:c.3603_3604delinsGA	ENSP00000379820.3:p.Gly1201=
ENST00000461292.3:n.3412-102_3412-101delinsGA
ENST00000535259.5:c.3362-102_3362-101delinsGA	ENSP00000441572.2:n.3362-102_3362-101delinsGA
ENST00000562109.5:c.3773-102_3773-101delinsGA	ENSP00000454998.1:n.3773-102_3773-101delinsGA
NM_000833.4:c.4014_4015delinsGA	NP_000824.1:p.Gly1338=
NM_001134407.2:c.4014_4015delinsGA	NP_001127879.1:p.Gly1338=
NM_001134408.2:c.3773-102_3773-101delinsGA	NP_001127880.1:n.3773-102_3773-101delinsGA
XM_011522456.1:c.3855_3856delinsGA	XP_011520758.1:p.Gly1285=
XM_011522457.1:c.3756_3757delinsGA	XP_011520759.1:p.Gly1252=
XM_011522458.1:c.3543_3544delinsGA	XP_011520760.1:p.Gly1181=
XM_011522459.1:c.3543_3544delinsGA	XP_011520761.1:p.Gly1181=
XM_011522460.1:c.3543_3544delinsGA	XP_011520762.1:p.Gly1181=
XM_011522461.1:c.3773-102_3773-101delinsGA	XP_011520763.1:n.3773-102_3773-101delinsGA
XM_011522458.3:c.3543_3544delinsGA	XP_011520760.1:p.Gly1181=
XM_011522461.3:c.3773-102_3773-101delinsGA	XP_011520763.1:n.3773-102_3773-101delinsGA
XM_017023172.1:c.4170_4171delinsGA	XP_016878661.1:p.Gly1390=
XM_017023173.1:c.3929-102_3929-101delinsGA	XP_016878662.1:n.3929-102_3929-101delinsGA
NM_001134407.3:c.4014_4015delinsGA MANE Select	NP_001127879.1:p.Gly1338=
NM_000833.5:c.4014_4015delinsGA	NP_000824.1:p.Gly1338=