Canonical Allele Identifier: CA2206692756
Gene: GRIN2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9763522_9763523delinsCT , CM000678.2:g.9763522_9763523delinsCT GRCh38
NC_000016.9:g.9857379_9857380delinsCT , CM000678.1:g.9857379_9857380delinsCT GRCh37
NC_000016.8:g.9764880_9764881delinsCT NCBI36
NG_011812.1:g.424232_424233delinsAG
NG_011812.2:g.424232_424233delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.4021_4022delinsAG MANE Select ENSP00000332549.3:p.Ser1341=
ENST00000535259.6:c.3302-95_3302-94delinsAG ENSP00000441572.3:n.3302-95_3302-94delinsAG
ENST00000636273.2:n.3366-95_3366-94delinsAG
ENST00000674742.1:c.3550_3551delinsAG ENSP00000502200.1:p.Ser1184=
ENST00000675398.1:c.*1391_*1392delinsAG ENSP00000502752.1:n.*1391_*1392delinsAG
ENST00000330684.3:c.4021_4022delinsAG ENSP00000332549.3:p.Ser1341=
ENST00000396573.6:c.4021_4022delinsAG ENSP00000379818.2:p.Ser1341=
ENST00000396575.6:c.3610_3611delinsAG ENSP00000379820.3:p.Ser1204=
ENST00000461292.3:n.3412-95_3412-94delinsAG
ENST00000535259.5:c.3362-95_3362-94delinsAG ENSP00000441572.2:n.3362-95_3362-94delinsAG
ENST00000562109.5:c.3773-95_3773-94delinsAG ENSP00000454998.1:n.3773-95_3773-94delinsAG
NM_000833.4:c.4021_4022delinsAG NP_000824.1:p.Ser1341=
NM_001134407.2:c.4021_4022delinsAG NP_001127879.1:p.Ser1341=
NM_001134408.2:c.3773-95_3773-94delinsAG NP_001127880.1:n.3773-95_3773-94delinsAG
XM_011522456.1:c.3862_3863delinsAG XP_011520758.1:p.Ser1288=
XM_011522457.1:c.3763_3764delinsAG XP_011520759.1:p.Ser1255=
XM_011522458.1:c.3550_3551delinsAG XP_011520760.1:p.Ser1184=
XM_011522459.1:c.3550_3551delinsAG XP_011520761.1:p.Ser1184=
XM_011522460.1:c.3550_3551delinsAG XP_011520762.1:p.Ser1184=
XM_011522461.1:c.3773-95_3773-94delinsAG XP_011520763.1:n.3773-95_3773-94delinsAG
XM_011522458.3:c.3550_3551delinsAG XP_011520760.1:p.Ser1184=
XM_011522461.3:c.3773-95_3773-94delinsAG XP_011520763.1:n.3773-95_3773-94delinsAG
XM_017023172.1:c.4177_4178delinsAG XP_016878661.1:p.Ser1393=
XM_017023173.1:c.3929-95_3929-94delinsAG XP_016878662.1:n.3929-95_3929-94delinsAG
NM_001134407.3:c.4021_4022delinsAG MANE Select NP_001127879.1:p.Ser1341=
NM_000833.5:c.4021_4022delinsAG NP_000824.1:p.Ser1341=