Canonical Allele Identifier: CA2805831322

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180117_10180118del , CM000678.2:g.10180117_10180118del	GRCh38
NC_000016.9:g.10273974_10273975del , CM000678.1:g.10273974_10273975del	GRCh37
NC_000016.8:g.10181475_10181476del	NCBI36
NG_011812.1:g.7637_7638del
NG_011812.2:g.7637_7638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.294_295del MANE Select	ENSP00000332549.3:p.Phe100TrpfsTer?
ENST00000675189.1:n.778_779del
ENST00000675398.1:c.294_295del	ENSP00000502752.1:p.Phe100TrpfsTer?
ENST00000676032.1:n.727_728del
ENST00000330684.3:c.294_295del	ENSP00000332549.3:p.Phe100TrpfsTer?
ENST00000396573.6:c.294_295del	ENSP00000379818.2:p.Phe100TrpfsTer?
ENST00000562109.5:c.294_295del	ENSP00000454998.1:p.Phe100TrpfsTer?
ENST00000566665.1:n.695_696del
NM_000833.4:c.294_295del	NP_000824.1:p.Phe100TrpfsTer?
NM_001134407.2:c.294_295del	NP_001127879.1:p.Phe100TrpfsTer?
NM_001134408.2:c.294_295del	NP_001127880.1:p.Phe100TrpfsTer?
XM_011522461.1:c.294_295del	XP_011520763.1:p.Phe100TrpfsTer?
XM_011522461.3:c.294_295del	XP_011520763.1:p.Phe100TrpfsTer?
XM_017023172.1:c.450_451del	XP_016878661.1:p.Phe152TrpfsTer?
XM_017023173.1:c.450_451del	XP_016878662.1:p.Phe152TrpfsTer?
NM_001134407.3:c.294_295del MANE Select	NP_001127879.1:p.Phe100TrpfsTer?
NM_000833.5:c.294_295del	NP_000824.1:p.Phe100TrpfsTer?