Canonical Allele Identifier: CA2731686183
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs2141127009

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9763485_9763493del , CM000678.2:g.9763485_9763493del GRCh38
NC_000016.9:g.9857342_9857350del , CM000678.1:g.9857342_9857350del GRCh37
NC_000016.8:g.9764843_9764851del NCBI36
NG_011812.1:g.424268_424276del
NG_011812.2:g.424268_424276del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.4057_4065del MANE Select ENSP00000332549.3:p.Arg1353_Lys1355del
ENST00000535259.6:c.3302-59_3302-51del ENSP00000441572.3:n.3302-59_3302-51del
ENST00000636273.2:n.3366-59_3366-51del
ENST00000674742.1:c.3586_3594del ENSP00000502200.1:p.Arg1196_Lys1198del
ENST00000675398.1:c.*1427_*1435del ENSP00000502752.1:n.*1427_*1435del
ENST00000330684.3:c.4057_4065del ENSP00000332549.3:p.Arg1353_Lys1355del
ENST00000396573.6:c.4057_4065del ENSP00000379818.2:p.Arg1353_Lys1355del
ENST00000396575.6:c.3646_3654del ENSP00000379820.3:p.Arg1216_Lys1218del
ENST00000461292.3:n.3412-59_3412-51del
ENST00000535259.5:c.3362-59_3362-51del ENSP00000441572.2:n.3362-59_3362-51del
ENST00000562109.5:c.3773-59_3773-51del ENSP00000454998.1:n.3773-59_3773-51del
NM_000833.4:c.4057_4065del NP_000824.1:p.Arg1353_Lys1355del
NM_001134407.2:c.4057_4065del NP_001127879.1:p.Arg1353_Lys1355del
NM_001134408.2:c.3773-59_3773-51del NP_001127880.1:n.3773-59_3773-51del
XM_011522456.1:c.3898_3906del XP_011520758.1:p.Arg1300_Lys1302del
XM_011522457.1:c.3799_3807del XP_011520759.1:p.Arg1267_Lys1269del
XM_011522458.1:c.3586_3594del XP_011520760.1:p.Arg1196_Lys1198del
XM_011522459.1:c.3586_3594del XP_011520761.1:p.Arg1196_Lys1198del
XM_011522460.1:c.3586_3594del XP_011520762.1:p.Arg1196_Lys1198del
XM_011522461.1:c.3773-59_3773-51del XP_011520763.1:n.3773-59_3773-51del
XM_011522458.3:c.3586_3594del XP_011520760.1:p.Arg1196_Lys1198del
XM_011522461.3:c.3773-59_3773-51del XP_011520763.1:n.3773-59_3773-51del
XM_017023172.1:c.4213_4221del XP_016878661.1:p.Arg1405_Lys1407del
XM_017023173.1:c.3929-59_3929-51del XP_016878662.1:n.3929-59_3929-51del
NM_001134407.3:c.4057_4065del MANE Select NP_001127879.1:p.Arg1353_Lys1355del
NM_000833.5:c.4057_4065del NP_000824.1:p.Arg1353_Lys1355del