Canonical Allele Identifier: CA2206692625

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763237T= , CM000678.2:g.9763237T=	GRCh38
NC_000016.9:g.9857094T= , CM000678.1:g.9857094T=	GRCh37
NC_000016.8:g.9764595T=	NCBI36
NG_011812.1:g.424518A=
NG_011812.2:g.424518A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.4307A= MANE Select	ENSP00000332549.3:p.Asn1436=
ENST00000535259.6:c.*118A=	ENSP00000441572.3:n.*118A=
ENST00000636273.2:n.3557A=
ENST00000674742.1:c.3836A=	ENSP00000502200.1:p.Asn1279=
ENST00000675398.1:c.*1677A=	ENSP00000502752.1:n.*1677A=
ENST00000330684.3:c.4307A=	ENSP00000332549.3:p.Asn1436=
ENST00000396573.6:c.4307A=	ENSP00000379818.2:p.Asn1436=
ENST00000396575.6:c.3896A=	ENSP00000379820.3:p.Asn1299=
ENST00000461292.3:n.3603A=
ENST00000535259.5:c.*118A=	ENSP00000441572.2:n.*118A=
ENST00000562109.5:c.*118A=	ENSP00000454998.1:n.*118A=
NM_000833.4:c.4307A=	NP_000824.1:p.Asn1436=
NM_001134407.2:c.4307A=	NP_001127879.1:p.Asn1436=
NM_001134408.2:c.*118A=	NP_001127880.1:n.*118A=
XM_011522456.1:c.4148A=	XP_011520758.1:p.Asn1383=
XM_011522457.1:c.4049A=	XP_011520759.1:p.Asn1350=
XM_011522458.1:c.3836A=	XP_011520760.1:p.Asn1279=
XM_011522459.1:c.3836A=	XP_011520761.1:p.Asn1279=
XM_011522460.1:c.3836A=	XP_011520762.1:p.Asn1279=
XM_011522461.1:c.*118A=	XP_011520763.1:n.*118A=
XM_011522458.3:c.3836A=	XP_011520760.1:p.Asn1279=
XM_011522461.3:c.*118A=	XP_011520763.1:n.*118A=
XM_017023172.1:c.4463A=	XP_016878661.1:p.Asn1488=
XM_017023173.1:c.*118A=	XP_016878662.1:n.*118A=
NM_001134407.3:c.4307A= MANE Select	NP_001127879.1:p.Asn1436=
NM_000833.5:c.4307A=	NP_000824.1:p.Asn1436=