Canonical Allele Identifier: CA2206912211

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10179949C= , CM000678.2:g.10179949C=	GRCh38
NC_000016.9:g.10273806C= , CM000678.1:g.10273806C=	GRCh37
NC_000016.8:g.10181307C=	NCBI36
NG_011812.1:g.7806G=
NG_011812.2:g.7806G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.414+49G= MANE Select	ENSP00000332549.3:n.414+49G=
ENST00000637334.1:n.93+49G=
ENST00000637393.1:c.6+49G=	ENSP00000490232.1:n.6+49G=
ENST00000675189.1:n.898+49G=
ENST00000675398.1:c.414+49G=	ENSP00000502752.1:n.414+49G=
ENST00000676032.1:n.896G=
ENST00000330684.3:c.414+49G=	ENSP00000332549.3:n.414+49G=
ENST00000396573.6:c.414+49G=	ENSP00000379818.2:n.414+49G=
ENST00000562109.5:c.414+49G=	ENSP00000454998.1:n.414+49G=
ENST00000566665.1:n.864G=
NM_000833.4:c.414+49G=	NP_000824.1:n.414+49G=
NM_001134407.2:c.414+49G=	NP_001127879.1:n.414+49G=
NM_001134408.2:c.414+49G=	NP_001127880.1:n.414+49G=
XM_011522461.1:c.414+49G=	XP_011520763.1:n.414+49G=
XM_011522461.3:c.414+49G=	XP_011520763.1:n.414+49G=
XM_017023172.1:c.570+49G=	XP_016878661.1:n.570+49G=
XM_017023173.1:c.570+49G=	XP_016878662.1:n.570+49G=
NM_001134407.3:c.414+49G= MANE Select	NP_001127879.1:n.414+49G=
NM_000833.5:c.414+49G=	NP_000824.1:n.414+49G=