Canonical Allele Identifier: CA2206912906

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180328_10180329delinsCT , CM000678.2:g.10180328_10180329delinsCT	GRCh38
NC_000016.9:g.10274185_10274186delinsCT , CM000678.1:g.10274185_10274186delinsCT	GRCh37
NC_000016.8:g.10181686_10181687delinsCT	NCBI36
NG_011812.1:g.7426_7427delinsAG
NG_011812.2:g.7426_7427delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.83_84delinsAG MANE Select	ENSP00000332549.3:p.Glu28=
ENST00000675189.1:n.567_568delinsAG
ENST00000675398.1:c.83_84delinsAG	ENSP00000502752.1:p.Glu28=
ENST00000676032.1:n.516_517delinsAG
ENST00000330684.3:c.83_84delinsAG	ENSP00000332549.3:p.Glu28=
ENST00000396573.6:c.83_84delinsAG	ENSP00000379818.2:p.Glu28=
ENST00000562109.5:c.83_84delinsAG	ENSP00000454998.1:p.Glu28=
ENST00000566665.1:n.484_485delinsAG
NM_000833.4:c.83_84delinsAG	NP_000824.1:p.Glu28=
NM_001134407.2:c.83_84delinsAG	NP_001127879.1:p.Glu28=
NM_001134408.2:c.83_84delinsAG	NP_001127880.1:p.Glu28=
XM_011522461.1:c.83_84delinsAG	XP_011520763.1:p.Glu28=
XM_011522461.3:c.83_84delinsAG	XP_011520763.1:p.Glu28=
XM_017023172.1:c.239_240delinsAG	XP_016878661.1:p.Glu80=
XM_017023173.1:c.239_240delinsAG	XP_016878662.1:p.Glu80=
NM_001134407.3:c.83_84delinsAG MANE Select	NP_001127879.1:p.Glu28=
NM_000833.5:c.83_84delinsAG	NP_000824.1:p.Glu28=