Canonical Allele Identifier: CA2842027279

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180390del , CM000678.2:g.10180390del	GRCh38
NC_000016.9:g.10274247del , CM000678.1:g.10274247del	GRCh37
NC_000016.8:g.10181748del	NCBI36
NG_011812.1:g.7365del
NG_011812.2:g.7365del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.22del MANE Select	ENSP00000332549.3:p.Thr8ProfsTer27
ENST00000636406.1:c.22del	ENSP00000490676.1:p.Thr8ProfsTer?
ENST00000637188.1:c.22del	ENSP00000489946.1:p.Thr8ProfsTer?
ENST00000675189.1:n.506del
ENST00000675398.1:c.22del	ENSP00000502752.1:p.Thr8ProfsTer27
ENST00000676032.1:n.455del
ENST00000330684.3:c.22del	ENSP00000332549.3:p.Thr8ProfsTer27
ENST00000396573.6:c.22del	ENSP00000379818.2:p.Thr8ProfsTer27
ENST00000562109.5:c.22del	ENSP00000454998.1:p.Thr8ProfsTer27
ENST00000566665.1:n.423del
NM_000833.4:c.22del	NP_000824.1:p.Thr8ProfsTer27
NM_001134407.2:c.22del	NP_001127879.1:p.Thr8ProfsTer27
NM_001134408.2:c.22del	NP_001127880.1:p.Thr8ProfsTer27
XM_011522461.1:c.22del	XP_011520763.1:p.Thr8ProfsTer27
XM_011522461.3:c.22del	XP_011520763.1:p.Thr8ProfsTer27
XM_017023172.1:c.178del	XP_016878661.1:p.Thr60ProfsTer27
XM_017023173.1:c.178del	XP_016878662.1:p.Thr60ProfsTer27
NM_001134407.3:c.22del MANE Select	NP_001127879.1:p.Thr8ProfsTer27
NM_000833.5:c.22del	NP_000824.1:p.Thr8ProfsTer27