Canonical Allele Identifier: CA2206693466

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9764883_9764884delinsCA , CM000678.2:g.9764883_9764884delinsCA	GRCh38
NC_000016.9:g.9858740_9858741delinsCA , CM000678.1:g.9858740_9858741delinsCA	GRCh37
NC_000016.8:g.9766241_9766242delinsCA	NCBI36
NG_011812.1:g.422871_422872delinsTG
NG_011812.2:g.422871_422872delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.2660_2661delinsTG MANE Select	ENSP00000332549.3:p.Leu887=
ENST00000535259.6:c.2189_2190delinsTG	ENSP00000441572.3:p.Leu730=
ENST00000636273.2:n.2253_2254delinsTG
ENST00000674742.1:c.2189_2190delinsTG	ENSP00000502200.1:p.Leu730=
ENST00000675398.1:c.*30_*31delinsTG	ENSP00000502752.1:n.*30_*31delinsTG
ENST00000330684.3:c.2660_2661delinsTG	ENSP00000332549.3:p.Leu887=
ENST00000396573.6:c.2660_2661delinsTG	ENSP00000379818.2:p.Leu887=
ENST00000396575.6:c.2249_2250delinsTG	ENSP00000379820.3:p.Leu750=
ENST00000461292.3:n.2299_2300delinsTG
ENST00000463531.1:n.443_444delinsTG
ENST00000535259.5:c.2249_2250delinsTG	ENSP00000441572.2:p.Leu750=
ENST00000562109.5:c.2660_2661delinsTG	ENSP00000454998.1:p.Leu887=
NM_000833.4:c.2660_2661delinsTG	NP_000824.1:p.Leu887=
NM_001134407.2:c.2660_2661delinsTG	NP_001127879.1:p.Leu887=
NM_001134408.2:c.2660_2661delinsTG	NP_001127880.1:p.Leu887=
XM_011522456.1:c.2501_2502delinsTG	XP_011520758.1:p.Leu834=
XM_011522457.1:c.2402_2403delinsTG	XP_011520759.1:p.Leu801=
XM_011522458.1:c.2189_2190delinsTG	XP_011520760.1:p.Leu730=
XM_011522459.1:c.2189_2190delinsTG	XP_011520761.1:p.Leu730=
XM_011522460.1:c.2189_2190delinsTG	XP_011520762.1:p.Leu730=
XM_011522461.1:c.2660_2661delinsTG	XP_011520763.1:p.Leu887=
XM_011522458.3:c.2189_2190delinsTG	XP_011520760.1:p.Leu730=
XM_011522461.3:c.2660_2661delinsTG	XP_011520763.1:p.Leu887=
XM_017023172.1:c.2816_2817delinsTG	XP_016878661.1:p.Leu939=
XM_017023173.1:c.2816_2817delinsTG	XP_016878662.1:p.Leu939=
NM_001134407.3:c.2660_2661delinsTG MANE Select	NP_001127879.1:p.Leu887=
NM_000833.5:c.2660_2661delinsTG	NP_000824.1:p.Leu887=