Canonical Allele Identifier: CA2631681621

Gene: GRIN2A

Linked Data

• gnomAD v4: 16-10180366-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180368del , CM000678.2:g.10180368del	GRCh38
NC_000016.9:g.10274225del , CM000678.1:g.10274225del	GRCh37
NC_000016.8:g.10181726del	NCBI36
NG_011812.1:g.7388del
NG_011812.2:g.7388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.45del MANE Select	ENSP00000332549.3:p.Leu16TrpfsTer19
ENST00000636406.1:c.45del	ENSP00000490676.1:p.Leu16TrpfsTer?
ENST00000675189.1:n.529del
ENST00000675398.1:c.45del	ENSP00000502752.1:p.Leu16TrpfsTer19
ENST00000676032.1:n.478del
ENST00000330684.3:c.45del	ENSP00000332549.3:p.Leu16TrpfsTer19
ENST00000396573.6:c.45del	ENSP00000379818.2:p.Leu16TrpfsTer19
ENST00000562109.5:c.45del	ENSP00000454998.1:p.Leu16TrpfsTer19
ENST00000566665.1:n.446del
NM_000833.4:c.45del	NP_000824.1:p.Leu16TrpfsTer19
NM_001134407.2:c.45del	NP_001127879.1:p.Leu16TrpfsTer19
NM_001134408.2:c.45del	NP_001127880.1:p.Leu16TrpfsTer19
XM_011522461.1:c.45del	XP_011520763.1:p.Leu16TrpfsTer19
XM_011522461.3:c.45del	XP_011520763.1:p.Leu16TrpfsTer19
XM_017023172.1:c.201del	XP_016878661.1:p.Leu68TrpfsTer19
XM_017023173.1:c.201del	XP_016878662.1:p.Leu68TrpfsTer19
NM_001134407.3:c.45del MANE Select	NP_001127879.1:p.Leu16TrpfsTer19
NM_000833.5:c.45del	NP_000824.1:p.Leu16TrpfsTer19