Canonical Allele Identifier: CA2206693100
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764196_9764199delinsCTTG , CM000678.2:g.9764196_9764199delinsCTTG GRCh38
NC_000016.9:g.9858053_9858056delinsCTTG , CM000678.1:g.9858053_9858056delinsCTTG GRCh37
NC_000016.8:g.9765554_9765557delinsCTTG NCBI36
NG_011812.1:g.423556_423559delinsCAAG
NG_011812.2:g.423556_423559delinsCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.3345_3348delinsCAAG MANE Select ENSP00000332549.3:p.Asp1115=
ENST00000535259.6:c.2874_2877delinsCAAG ENSP00000441572.3:p.Asp958=
ENST00000636273.2:n.2938_2941delinsCAAG
ENST00000674742.1:c.2874_2877delinsCAAG ENSP00000502200.1:p.Asp958=
ENST00000675398.1:c.*715_*718delinsCAAG ENSP00000502752.1:n.*715_*718delinsCAAG
ENST00000330684.3:c.3345_3348delinsCAAG ENSP00000332549.3:p.Asp1115=
ENST00000396573.6:c.3345_3348delinsCAAG ENSP00000379818.2:p.Asp1115=
ENST00000396575.6:c.2934_2937delinsCAAG ENSP00000379820.3:p.Asp978=
ENST00000461292.3:n.2984_2987delinsCAAG
ENST00000535259.5:c.2934_2937delinsCAAG ENSP00000441572.2:p.Asp978=
ENST00000562109.5:c.3345_3348delinsCAAG ENSP00000454998.1:p.Asp1115=
NM_000833.4:c.3345_3348delinsCAAG NP_000824.1:p.Asp1115=
NM_001134407.2:c.3345_3348delinsCAAG NP_001127879.1:p.Asp1115=
NM_001134408.2:c.3345_3348delinsCAAG NP_001127880.1:p.Asp1115=
XM_011522456.1:c.3186_3189delinsCAAG XP_011520758.1:p.Asp1062=
XM_011522457.1:c.3087_3090delinsCAAG XP_011520759.1:p.Asp1029=
XM_011522458.1:c.2874_2877delinsCAAG XP_011520760.1:p.Asp958=
XM_011522459.1:c.2874_2877delinsCAAG XP_011520761.1:p.Asp958=
XM_011522460.1:c.2874_2877delinsCAAG XP_011520762.1:p.Asp958=
XM_011522461.1:c.3345_3348delinsCAAG XP_011520763.1:p.Asp1115=
XM_011522458.3:c.2874_2877delinsCAAG XP_011520760.1:p.Asp958=
XM_011522461.3:c.3345_3348delinsCAAG XP_011520763.1:p.Asp1115=
XM_017023172.1:c.3501_3504delinsCAAG XP_016878661.1:p.Asp1167=
XM_017023173.1:c.3501_3504delinsCAAG XP_016878662.1:p.Asp1167=
NM_001134407.3:c.3345_3348delinsCAAG MANE Select NP_001127879.1:p.Asp1115=
NM_000833.5:c.3345_3348delinsCAAG NP_000824.1:p.Asp1115=