Canonical Allele Identifier: CA2206912665

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180213C= , CM000678.2:g.10180213C=	GRCh38
NC_000016.9:g.10274070C= , CM000678.1:g.10274070C=	GRCh37
NC_000016.8:g.10181571C=	NCBI36
NG_011812.1:g.7542G=
NG_011812.2:g.7542G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.199G= MANE Select	ENSP00000332549.3:p.Val67=
ENST00000675189.1:n.683G=
ENST00000675398.1:c.199G=	ENSP00000502752.1:p.Val67=
ENST00000676032.1:n.632G=
ENST00000330684.3:c.199G=	ENSP00000332549.3:p.Val67=
ENST00000396573.6:c.199G=	ENSP00000379818.2:p.Val67=
ENST00000562109.5:c.199G=	ENSP00000454998.1:p.Val67=
ENST00000566665.1:n.600G=
NM_000833.4:c.199G=	NP_000824.1:p.Val67=
NM_001134407.2:c.199G=	NP_001127879.1:p.Val67=
NM_001134408.2:c.199G=	NP_001127880.1:p.Val67=
XM_011522461.1:c.199G=	XP_011520763.1:p.Val67=
XM_011522461.3:c.199G=	XP_011520763.1:p.Val67=
XM_017023172.1:c.355G=	XP_016878661.1:p.Val119=
XM_017023173.1:c.355G=	XP_016878662.1:p.Val119=
NM_001134407.3:c.199G= MANE Select	NP_001127879.1:p.Val67=
NM_000833.5:c.199G=	NP_000824.1:p.Val67=