Canonical Allele Identifier: CA2206782748

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9938372C= , CM000678.2:g.9938372C=	GRCh38
NC_000016.9:g.10032229C= , CM000678.1:g.10032229C=	GRCh37
NC_000016.8:g.9939730C=	NCBI36
NG_011812.1:g.249383G=
NG_011812.2:g.249383G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.594G= MANE Select	ENSP00000332549.3:p.Trp198=
ENST00000535259.6:c.123G=	ENSP00000441572.3:p.Trp41=
ENST00000636273.2:n.187G=
ENST00000637393.1:c.186G=	ENSP00000490232.1:p.Trp62=
ENST00000674742.1:c.123G=	ENSP00000502200.1:p.Trp41=
ENST00000675189.1:n.1078G=
ENST00000675398.1:c.594G=	ENSP00000502752.1:p.Trp198=
ENST00000330684.3:c.594G=	ENSP00000332549.3:p.Trp198=
ENST00000396573.6:c.594G=	ENSP00000379818.2:p.Trp198=
ENST00000396575.6:c.183G=	ENSP00000379820.3:p.Trp61=
ENST00000461292.3:n.233G=
ENST00000535259.5:c.183G=	ENSP00000441572.2:p.Trp61=
ENST00000562109.5:c.594G=	ENSP00000454998.1:p.Trp198=
ENST00000566670.2:n.436G=
ENST00000566683.1:n.241-47272G=
ENST00000568247.3:n.486G=
NM_000833.4:c.594G=	NP_000824.1:p.Trp198=
NM_001134407.2:c.594G=	NP_001127879.1:p.Trp198=
NM_001134408.2:c.594G=	NP_001127880.1:p.Trp198=
XM_011522456.1:c.435G=	XP_011520758.1:p.Trp145=
XM_011522457.1:c.336G=	XP_011520759.1:p.Trp112=
XM_011522458.1:c.123G=	XP_011520760.1:p.Trp41=
XM_011522459.1:c.123G=	XP_011520761.1:p.Trp41=
XM_011522460.1:c.123G=	XP_011520762.1:p.Trp41=
XM_011522461.1:c.594G=	XP_011520763.1:p.Trp198=
XM_011522458.3:c.123G=	XP_011520760.1:p.Trp41=
XM_011522461.3:c.594G=	XP_011520763.1:p.Trp198=
XM_017023172.1:c.750G=	XP_016878661.1:p.Trp250=
XM_017023173.1:c.750G=	XP_016878662.1:p.Trp250=
NM_001134407.3:c.594G= MANE Select	NP_001127879.1:p.Trp198=
NM_000833.5:c.594G=	NP_000824.1:p.Trp198=