Canonical Allele Identifier: CA2206693104

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764199_9764217delinsGTCTCTAGGGGAGCTTGAT , CM000678.2:g.9764199_9764217delinsGTCTCTAGGGGAGCTTGAT	GRCh38
NC_000016.9:g.9858056_9858074delinsGTCTCTAGGGGAGCTTGAT , CM000678.1:g.9858056_9858074delinsGTCTCTAGGGGAGCTTGAT	GRCh37
NC_000016.8:g.9765557_9765575delinsGTCTCTAGGGGAGCTTGAT	NCBI36
NG_011812.1:g.423538_423556delinsATCAAGCTCCCCTAGAGAC
NG_011812.2:g.423538_423556delinsATCAAGCTCCCCTAGAGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.3327_3345delinsATCAAGCTCCCCTAGAGAC MANE Select	ENSP00000332549.3:p.Lys1109=
ENST00000535259.6:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	ENSP00000441572.3:p.Lys952=
ENST00000636273.2:n.2920_2938delinsATCAAGCTCCCCTAGAGAC
ENST00000674742.1:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	ENSP00000502200.1:p.Lys952=
ENST00000675398.1:c.*697_*715delinsATCAAGCTCCCCTAGAGAC	ENSP00000502752.1:n.*697_*715delinsATCAAGCTCCCCTAGAGAC
ENST00000330684.3:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	ENSP00000332549.3:p.Lys1109=
ENST00000396573.6:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	ENSP00000379818.2:p.Lys1109=
ENST00000396575.6:c.2916_2934delinsATCAAGCTCCCCTAGAGAC	ENSP00000379820.3:p.Lys972=
ENST00000461292.3:n.2966_2984delinsATCAAGCTCCCCTAGAGAC
ENST00000535259.5:c.2916_2934delinsATCAAGCTCCCCTAGAGAC	ENSP00000441572.2:p.Lys972=
ENST00000562109.5:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	ENSP00000454998.1:p.Lys1109=
NM_000833.4:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	NP_000824.1:p.Lys1109=
NM_001134407.2:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	NP_001127879.1:p.Lys1109=
NM_001134408.2:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	NP_001127880.1:p.Lys1109=
XM_011522456.1:c.3168_3186delinsATCAAGCTCCCCTAGAGAC	XP_011520758.1:p.Lys1056=
XM_011522457.1:c.3069_3087delinsATCAAGCTCCCCTAGAGAC	XP_011520759.1:p.Lys1023=
XM_011522458.1:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	XP_011520760.1:p.Lys952=
XM_011522459.1:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	XP_011520761.1:p.Lys952=
XM_011522460.1:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	XP_011520762.1:p.Lys952=
XM_011522461.1:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	XP_011520763.1:p.Lys1109=
XM_011522458.3:c.2856_2874delinsATCAAGCTCCCCTAGAGAC	XP_011520760.1:p.Lys952=
XM_011522461.3:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	XP_011520763.1:p.Lys1109=
XM_017023172.1:c.3483_3501delinsATCAAGCTCCCCTAGAGAC	XP_016878661.1:p.Lys1161=
XM_017023173.1:c.3483_3501delinsATCAAGCTCCCCTAGAGAC	XP_016878662.1:p.Lys1161=
NM_001134407.3:c.3327_3345delinsATCAAGCTCCCCTAGAGAC MANE Select	NP_001127879.1:p.Lys1109=
NM_000833.5:c.3327_3345delinsATCAAGCTCCCCTAGAGAC	NP_000824.1:p.Lys1109=