Canonical Allele Identifier: CA2842027278
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10180357_10180358del , CM000678.2:g.10180357_10180358del GRCh38
NC_000016.9:g.10274214_10274215del , CM000678.1:g.10274214_10274215del GRCh37
NC_000016.8:g.10181715_10181716del NCBI36
NG_011812.1:g.7400_7401del
NG_011812.2:g.7400_7401del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.57_58del MANE Select ENSP00000332549.3:p.Gly20SerfsTer?
ENST00000636406.1:c.57_58del ENSP00000490676.1:p.Arg19=
ENST00000675189.1:n.541_542del
ENST00000675398.1:c.57_58del ENSP00000502752.1:p.Gly20SerfsTer?
ENST00000676032.1:n.490_491del
ENST00000330684.3:c.57_58del ENSP00000332549.3:p.Gly20SerfsTer?
ENST00000396573.6:c.57_58del ENSP00000379818.2:p.Gly20SerfsTer?
ENST00000562109.5:c.57_58del ENSP00000454998.1:p.Gly20SerfsTer?
ENST00000566665.1:n.458_459del
NM_000833.4:c.57_58del NP_000824.1:p.Gly20SerfsTer?
NM_001134407.2:c.57_58del NP_001127879.1:p.Gly20SerfsTer?
NM_001134408.2:c.57_58del NP_001127880.1:p.Gly20SerfsTer?
XM_011522461.1:c.57_58del XP_011520763.1:p.Gly20SerfsTer?
XM_011522461.3:c.57_58del XP_011520763.1:p.Gly20SerfsTer?
XM_017023172.1:c.213_214del XP_016878661.1:p.Gly72SerfsTer?
XM_017023173.1:c.213_214del XP_016878662.1:p.Gly72SerfsTer?
NM_001134407.3:c.57_58del MANE Select NP_001127879.1:p.Gly20SerfsTer?
NM_000833.5:c.57_58del NP_000824.1:p.Gly20SerfsTer?