Canonical Allele Identifier: CA2206912691

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180230G= , CM000678.2:g.10180230G=	GRCh38
NC_000016.9:g.10274087G= , CM000678.1:g.10274087G=	GRCh37
NC_000016.8:g.10181588G=	NCBI36
NG_011812.1:g.7525C=
NG_011812.2:g.7525C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.182C= MANE Select	ENSP00000332549.3:p.Ala61=
ENST00000675189.1:n.666C=
ENST00000675398.1:c.182C=	ENSP00000502752.1:p.Ala61=
ENST00000676032.1:n.615C=
ENST00000330684.3:c.182C=	ENSP00000332549.3:p.Ala61=
ENST00000396573.6:c.182C=	ENSP00000379818.2:p.Ala61=
ENST00000562109.5:c.182C=	ENSP00000454998.1:p.Ala61=
ENST00000566665.1:n.583C=
NM_000833.4:c.182C=	NP_000824.1:p.Ala61=
NM_001134407.2:c.182C=	NP_001127879.1:p.Ala61=
NM_001134408.2:c.182C=	NP_001127880.1:p.Ala61=
XM_011522461.1:c.182C=	XP_011520763.1:p.Ala61=
XM_011522461.3:c.182C=	XP_011520763.1:p.Ala61=
XM_017023172.1:c.338C=	XP_016878661.1:p.Ala113=
XM_017023173.1:c.338C=	XP_016878662.1:p.Ala113=
NM_001134407.3:c.182C= MANE Select	NP_001127879.1:p.Ala61=
NM_000833.5:c.182C=	NP_000824.1:p.Ala61=