Canonical Allele Identifier: CA2206782621

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938080T= , CM000678.2:g.9938080T=	GRCh38
NC_000016.9:g.10031937T= , CM000678.1:g.10031937T=	GRCh37
NC_000016.8:g.9939438T=	NCBI36
NG_011812.1:g.249675A=
NG_011812.2:g.249675A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.886A= MANE Select	ENSP00000332549.3:p.Ile296=
ENST00000535259.6:c.415A=	ENSP00000441572.3:p.Ile139=
ENST00000636273.2:n.479A=
ENST00000637393.1:c.478A=	ENSP00000490232.1:p.Ile160=
ENST00000674742.1:c.415A=	ENSP00000502200.1:p.Ile139=
ENST00000675189.1:n.1370A=
ENST00000675398.1:c.886A=	ENSP00000502752.1:p.Ile296=
ENST00000330684.3:c.886A=	ENSP00000332549.3:p.Ile296=
ENST00000396573.6:c.886A=	ENSP00000379818.2:p.Ile296=
ENST00000396575.6:c.475A=	ENSP00000379820.3:p.Ile159=
ENST00000461292.3:n.525A=
ENST00000535259.5:c.475A=	ENSP00000441572.2:p.Ile159=
ENST00000562109.5:c.886A=	ENSP00000454998.1:p.Ile296=
ENST00000566683.1:n.241-46980A=
ENST00000568247.3:n.778A=
NM_000833.4:c.886A=	NP_000824.1:p.Ile296=
NM_001134407.2:c.886A=	NP_001127879.1:p.Ile296=
NM_001134408.2:c.886A=	NP_001127880.1:p.Ile296=
XM_011522456.1:c.727A=	XP_011520758.1:p.Ile243=
XM_011522457.1:c.628A=	XP_011520759.1:p.Ile210=
XM_011522458.1:c.415A=	XP_011520760.1:p.Ile139=
XM_011522459.1:c.415A=	XP_011520761.1:p.Ile139=
XM_011522460.1:c.415A=	XP_011520762.1:p.Ile139=
XM_011522461.1:c.886A=	XP_011520763.1:p.Ile296=
XM_011522458.3:c.415A=	XP_011520760.1:p.Ile139=
XM_011522461.3:c.886A=	XP_011520763.1:p.Ile296=
XM_017023172.1:c.1042A=	XP_016878661.1:p.Ile348=
XM_017023173.1:c.1042A=	XP_016878662.1:p.Ile348=
NM_001134407.3:c.886A= MANE Select	NP_001127879.1:p.Ile296=
NM_000833.5:c.886A=	NP_000824.1:p.Ile296=