Canonical Allele Identifier: CA2206913169

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180420C= , CM000678.2:g.10180420C=	GRCh38
NC_000016.9:g.10274277C= , CM000678.1:g.10274277C=	GRCh37
NC_000016.8:g.10181778C=	NCBI36
NG_011812.1:g.7335G=
NG_011812.2:g.7335G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.-9G= MANE Select	ENSP00000332549.3:n.-9G=
ENST00000636406.1:c.-9G=	ENSP00000490676.1:n.-9G=
ENST00000637188.1:c.-9G=	ENSP00000489946.1:n.-9G=
ENST00000675189.1:n.476G=
ENST00000675398.1:c.-9G=	ENSP00000502752.1:n.-9G=
ENST00000676032.1:n.425G=
ENST00000330684.3:c.-9G=	ENSP00000332549.3:n.-9G=
ENST00000396573.6:c.-9G=	ENSP00000379818.2:n.-9G=
ENST00000562109.5:c.-9G=	ENSP00000454998.1:n.-9G=
ENST00000566665.1:n.393G=
NM_000833.4:c.-9G=	NP_000824.1:n.-9G=
NM_001134407.2:c.-9G=	NP_001127879.1:n.-9G=
NM_001134408.2:c.-9G=	NP_001127880.1:n.-9G=
XM_011522461.1:c.-9G=	XP_011520763.1:n.-9G=
XM_011522461.3:c.-9G=	XP_011520763.1:n.-9G=
XM_017023172.1:c.148G=	XP_016878661.1:p.Val50=
XM_017023173.1:c.148G=	XP_016878662.1:p.Val50=
NM_001134407.3:c.-9G= MANE Select	NP_001127879.1:n.-9G=
NM_000833.5:c.-9G=	NP_000824.1:n.-9G=