Canonical Allele Identifier: CA2206692577

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9763145A= , CM000678.2:g.9763145A=	GRCh38
NC_000016.9:g.9857002A= , CM000678.1:g.9857002A=	GRCh37
NC_000016.8:g.9764503A=	NCBI36
NG_011812.1:g.424610T=
NG_011812.2:g.424610T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.*4T= MANE Select	ENSP00000332549.3:n.*4T=
ENST00000535259.6:c.*210T=	ENSP00000441572.3:n.*210T=
ENST00000636273.2:n.3649T=
ENST00000674742.1:c.*4T=	ENSP00000502200.1:n.*4T=
ENST00000675398.1:c.*1769T=	ENSP00000502752.1:n.*1769T=
ENST00000330684.3:c.*4T=	ENSP00000332549.3:n.*4T=
ENST00000396573.6:c.*4T=	ENSP00000379818.2:n.*4T=
ENST00000396575.6:c.3988T=	ENSP00000379820.3:n.3988T=
ENST00000461292.3:n.3695T=
ENST00000535259.5:c.*210T=	ENSP00000441572.2:n.*210T=
ENST00000562109.5:c.*210T=	ENSP00000454998.1:n.*210T=
NM_000833.4:c.*4T=	NP_000824.1:n.*4T=
NM_001134407.2:c.*4T=	NP_001127879.1:n.*4T=
NM_001134408.2:c.*210T=	NP_001127880.1:n.*210T=
XM_011522456.1:c.*4T=	XP_011520758.1:n.*4T=
XM_011522457.1:c.*4T=	XP_011520759.1:n.*4T=
XM_011522458.1:c.*4T=	XP_011520760.1:n.*4T=
XM_011522459.1:c.*4T=	XP_011520761.1:n.*4T=
XM_011522460.1:c.*4T=	XP_011520762.1:n.*4T=
XM_011522461.1:c.*210T=	XP_011520763.1:n.*210T=
XM_011522458.3:c.*4T=	XP_011520760.1:n.*4T=
XM_011522461.3:c.*210T=	XP_011520763.1:n.*210T=
XM_017023172.1:c.*4T=	XP_016878661.1:n.*4T=
XM_017023173.1:c.*210T=	XP_016878662.1:n.*210T=
NM_001134407.3:c.*4T= MANE Select	NP_001127879.1:n.*4T=
NM_000833.5:c.*4T=	NP_000824.1:n.*4T=