Canonical Allele Identifier: CA2206913150

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180410A= , CM000678.2:g.10180410A=	GRCh38
NC_000016.9:g.10274267A= , CM000678.1:g.10274267A=	GRCh37
NC_000016.8:g.10181768A=	NCBI36
NG_011812.1:g.7345T=
NG_011812.2:g.7345T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.2T= MANE Select	ENSP00000332549.3:p.Met1=
ENST00000636406.1:c.2T=	ENSP00000490676.1:p.Met1=
ENST00000637188.1:c.2T=	ENSP00000489946.1:p.Met1=
ENST00000675189.1:n.486T=
ENST00000675398.1:c.2T=	ENSP00000502752.1:p.Met1=
ENST00000676032.1:n.435T=
ENST00000330684.3:c.2T=	ENSP00000332549.3:p.Met1=
ENST00000396573.6:c.2T=	ENSP00000379818.2:p.Met1=
ENST00000562109.5:c.2T=	ENSP00000454998.1:p.Met1=
ENST00000566665.1:n.403T=
NM_000833.4:c.2T=	NP_000824.1:p.Met1=
NM_001134407.2:c.2T=	NP_001127879.1:p.Met1=
NM_001134408.2:c.2T=	NP_001127880.1:p.Met1=
XM_011522461.1:c.2T=	XP_011520763.1:p.Met1=
XM_011522461.3:c.2T=	XP_011520763.1:p.Met1=
XM_017023172.1:c.158T=	XP_016878661.1:p.Met53=
XM_017023173.1:c.158T=	XP_016878662.1:p.Met53=
NM_001134407.3:c.2T= MANE Select	NP_001127879.1:p.Met1=
NM_000833.5:c.2T=	NP_000824.1:p.Met1=