Canonical Allele Identifier: CA2206912384

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180080T= , CM000678.2:g.10180080T=	GRCh38
NC_000016.9:g.10273937T= , CM000678.1:g.10273937T=	GRCh37
NC_000016.8:g.10181438T=	NCBI36
NG_011812.1:g.7675A=
NG_011812.2:g.7675A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.332A= MANE Select	ENSP00000332549.3:p.Gln111=
ENST00000637334.1:n.11A=
ENST00000675189.1:n.816A=
ENST00000675398.1:c.332A=	ENSP00000502752.1:p.Gln111=
ENST00000676032.1:n.765A=
ENST00000330684.3:c.332A=	ENSP00000332549.3:p.Gln111=
ENST00000396573.6:c.332A=	ENSP00000379818.2:p.Gln111=
ENST00000562109.5:c.332A=	ENSP00000454998.1:p.Gln111=
ENST00000566665.1:n.733A=
NM_000833.4:c.332A=	NP_000824.1:p.Gln111=
NM_001134407.2:c.332A=	NP_001127879.1:p.Gln111=
NM_001134408.2:c.332A=	NP_001127880.1:p.Gln111=
XM_011522461.1:c.332A=	XP_011520763.1:p.Gln111=
XM_011522461.3:c.332A=	XP_011520763.1:p.Gln111=
XM_017023172.1:c.488A=	XP_016878661.1:p.Gln163=
XM_017023173.1:c.488A=	XP_016878662.1:p.Gln163=
NM_001134407.3:c.332A= MANE Select	NP_001127879.1:p.Gln111=
NM_000833.5:c.332A=	NP_000824.1:p.Gln111=