Canonical Allele Identifier: CA2206912911

Gene: GRIN2A

Linked Data

• dbSNP Id: rs2050240263

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180329del , CM000678.2:g.10180329del	GRCh38
NC_000016.9:g.10274186del , CM000678.1:g.10274186del	GRCh37
NC_000016.8:g.10181687del	NCBI36
NG_011812.1:g.7426del
NG_011812.2:g.7426del

Transcript Alleles

HGVS	Amino-acid change
ENST00000330684.4:c.83del MANE Select	ENSP00000332549.3:p.Glu28GlyfsTer7
ENST00000675189.1:n.567del
ENST00000675398.1:c.83del	ENSP00000502752.1:p.Glu28GlyfsTer7
ENST00000676032.1:n.516del
ENST00000330684.3:c.83del	ENSP00000332549.3:p.Glu28GlyfsTer7
ENST00000396573.6:c.83del	ENSP00000379818.2:p.Glu28GlyfsTer7
ENST00000562109.5:c.83del	ENSP00000454998.1:p.Glu28GlyfsTer7
ENST00000566665.1:n.484del
NM_000833.4:c.83del	NP_000824.1:p.Glu28GlyfsTer7
NM_001134407.2:c.83del	NP_001127879.1:p.Glu28GlyfsTer7
NM_001134408.2:c.83del	NP_001127880.1:p.Glu28GlyfsTer7
XM_011522461.1:c.83del	XP_011520763.1:p.Glu28GlyfsTer7
XM_011522461.3:c.83del	XP_011520763.1:p.Glu28GlyfsTer7
XM_017023172.1:c.239del	XP_016878661.1:p.Glu80GlyfsTer7
XM_017023173.1:c.239del	XP_016878662.1:p.Glu80GlyfsTer7
NM_001134407.3:c.83del MANE Select	NP_001127879.1:p.Glu28GlyfsTer7
NM_000833.5:c.83del	NP_000824.1:p.Glu28GlyfsTer7