Canonical Allele Identifier: CA2206912797

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180275A= , CM000678.2:g.10180275A=	GRCh38
NC_000016.9:g.10274132A= , CM000678.1:g.10274132A=	GRCh37
NC_000016.8:g.10181633A=	NCBI36
NG_011812.1:g.7480T=
NG_011812.2:g.7480T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.137T= MANE Select	ENSP00000332549.3:p.Val46=
ENST00000675189.1:n.621T=
ENST00000675398.1:c.137T=	ENSP00000502752.1:p.Val46=
ENST00000676032.1:n.570T=
ENST00000330684.3:c.137T=	ENSP00000332549.3:p.Val46=
ENST00000396573.6:c.137T=	ENSP00000379818.2:p.Val46=
ENST00000562109.5:c.137T=	ENSP00000454998.1:p.Val46=
ENST00000566665.1:n.538T=
NM_000833.4:c.137T=	NP_000824.1:p.Val46=
NM_001134407.2:c.137T=	NP_001127879.1:p.Val46=
NM_001134408.2:c.137T=	NP_001127880.1:p.Val46=
XM_011522461.1:c.137T=	XP_011520763.1:p.Val46=
XM_011522461.3:c.137T=	XP_011520763.1:p.Val46=
XM_017023172.1:c.293T=	XP_016878661.1:p.Val98=
XM_017023173.1:c.293T=	XP_016878662.1:p.Val98=
NM_001134407.3:c.137T= MANE Select	NP_001127879.1:p.Val46=
NM_000833.5:c.137T=	NP_000824.1:p.Val46=