Canonical Allele Identifier: CA2805831321
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10180027dup , CM000678.2:g.10180027dup GRCh38
NC_000016.9:g.10273884dup , CM000678.1:g.10273884dup GRCh37
NC_000016.8:g.10181385dup NCBI36
NG_011812.1:g.7732dup
NG_011812.2:g.7732dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.389dup MANE Select ENSP00000332549.3:p.Ala131ArgfsTer7
ENST00000637334.1:n.68dup
ENST00000675189.1:n.873dup
ENST00000675398.1:c.389dup ENSP00000502752.1:p.Ala131ArgfsTer7
ENST00000676032.1:n.822dup
ENST00000330684.3:c.389dup ENSP00000332549.3:p.Ala131ArgfsTer7
ENST00000396573.6:c.389dup ENSP00000379818.2:p.Ala131ArgfsTer7
ENST00000562109.5:c.389dup ENSP00000454998.1:p.Ala131ArgfsTer7
ENST00000566665.1:n.790dup
NM_000833.4:c.389dup NP_000824.1:p.Ala131ArgfsTer7
NM_001134407.2:c.389dup NP_001127879.1:p.Ala131ArgfsTer7
NM_001134408.2:c.389dup NP_001127880.1:p.Ala131ArgfsTer7
XM_011522461.1:c.389dup XP_011520763.1:p.Ala131ArgfsTer7
XM_011522461.3:c.389dup XP_011520763.1:p.Ala131ArgfsTer7
XM_017023172.1:c.545dup XP_016878661.1:p.Ala183ArgfsTer7
XM_017023173.1:c.545dup XP_016878662.1:p.Ala183ArgfsTer7
NM_001134407.3:c.389dup MANE Select NP_001127879.1:p.Ala131ArgfsTer7
NM_000833.5:c.389dup NP_000824.1:p.Ala131ArgfsTer7