Canonical Allele Identifier: CA493693945

Gene: GRIN2A

Linked Data

• COSMIC: COSM311640
• MyVariant Identifiers: chr16:g.10273897del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180040del , CM000678.2:g.10180040del	GRCh38
NC_000016.9:g.10273897del , CM000678.1:g.10273897del	GRCh37
NC_000016.8:g.10181398del	NCBI36
NG_011812.1:g.7715del
NG_011812.2:g.7715del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.372del MANE Select	ENSP00000332549.3:p.Leu125TrpfsTer9
ENST00000637334.1:n.51del
ENST00000675189.1:n.856del
ENST00000675398.1:c.372del	ENSP00000502752.1:p.Leu125TrpfsTer9
ENST00000676032.1:n.805del
ENST00000330684.3:c.372del	ENSP00000332549.3:p.Leu125TrpfsTer9
ENST00000396573.6:c.372del	ENSP00000379818.2:p.Leu125TrpfsTer9
ENST00000562109.5:c.372del	ENSP00000454998.1:p.Leu125TrpfsTer9
ENST00000566665.1:n.773del
NM_000833.4:c.372del	NP_000824.1:p.Leu125TrpfsTer9
NM_001134407.2:c.372del	NP_001127879.1:p.Leu125TrpfsTer9
NM_001134408.2:c.372del	NP_001127880.1:p.Leu125TrpfsTer9
XM_011522461.1:c.372del	XP_011520763.1:p.Leu125TrpfsTer9
XM_011522461.3:c.372del	XP_011520763.1:p.Leu125TrpfsTer9
XM_017023172.1:c.528del	XP_016878661.1:p.Leu177TrpfsTer9
XM_017023173.1:c.528del	XP_016878662.1:p.Leu177TrpfsTer9
NM_001134407.3:c.372del MANE Select	NP_001127879.1:p.Leu125TrpfsTer9
NM_000833.5:c.372del	NP_000824.1:p.Leu125TrpfsTer9