Canonical Allele Identifier: CA2839807903

Gene: GRIN2A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10180392dup , CM000678.2:g.10180392dup	GRCh38
NC_000016.9:g.10274249dup , CM000678.1:g.10274249dup	GRCh37
NC_000016.8:g.10181750dup	NCBI36
NG_011812.1:g.7364dup
NG_011812.2:g.7364dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330684.4:c.21dup MANE Select	ENSP00000332549.3:p.Thr8AspfsTer?
ENST00000636406.1:c.21dup	ENSP00000490676.1:p.Thr8AspfsTer?
ENST00000637188.1:c.21dup	ENSP00000489946.1:p.Thr8AspfsTer?
ENST00000675189.1:n.505dup
ENST00000675398.1:c.21dup	ENSP00000502752.1:p.Thr8AspfsTer?
ENST00000676032.1:n.454dup
ENST00000330684.3:c.21dup	ENSP00000332549.3:p.Thr8AspfsTer?
ENST00000396573.6:c.21dup	ENSP00000379818.2:p.Thr8AspfsTer?
ENST00000562109.5:c.21dup	ENSP00000454998.1:p.Thr8AspfsTer?
ENST00000566665.1:n.422dup
NM_000833.4:c.21dup	NP_000824.1:p.Thr8AspfsTer?
NM_001134407.2:c.21dup	NP_001127879.1:p.Thr8AspfsTer?
NM_001134408.2:c.21dup	NP_001127880.1:p.Thr8AspfsTer?
XM_011522461.1:c.21dup	XP_011520763.1:p.Thr8AspfsTer?
XM_011522461.3:c.21dup	XP_011520763.1:p.Thr8AspfsTer?
XM_017023172.1:c.177dup	XP_016878661.1:p.Thr60AspfsTer?
XM_017023173.1:c.177dup	XP_016878662.1:p.Thr60AspfsTer?
NM_001134407.3:c.21dup MANE Select	NP_001127879.1:p.Thr8AspfsTer?
NM_000833.5:c.21dup	NP_000824.1:p.Thr8AspfsTer?