Canonical Allele Identifier: CA14294171
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs4998386

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9976688C>T , CM000678.2:g.9976688C>T GRCh38
NC_000016.9:g.10070545C>T , CM000678.1:g.10070545C>T GRCh37
NC_000016.8:g.9978046C>T NCBI36
NG_011812.1:g.211067G>A
NG_011812.2:g.211067G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.415-38137G>A MANE Select ENSP00000332549.3:p.=
ENST00000637393.1:n.7-38137G>A ENSP00000490232.1:p.=
ENST00000674742.1:c.-57-38137G>A ENSP00000502200.1:p.=
ENST00000675189.1:n.899-38137G>A
ENST00000675398.1:c.415-38137G>A ENSP00000502752.1:p.=
ENST00000330684.3:c.415-38137G>A ENSP00000332549.3:p.=
ENST00000396573.6:c.415-38137G>A ENSP00000379818.2:p.=
ENST00000562109.5:c.415-38137G>A ENSP00000454998.1:p.=
ENST00000566670.2:n.257-38137G>A
ENST00000566683.1:n.240+54637G>A
ENST00000568247.3:n.141-33392G>A
NM_000833.4:c.415-38137G>A NP_000824.1:p.=
NM_001134407.2:c.415-38137G>A NP_001127879.1:p.=
NM_001134408.2:c.415-38137G>A NP_001127880.1:p.=
XM_011522456.1:c.256-38137G>A XP_011520758.1:p.=
XM_011522458.1:c.-57-38137G>A XP_011520760.1:p.=
XM_011522459.1:c.-201-21988G>A XP_011520761.1:p.=
XM_011522460.1:c.-197-21992G>A XP_011520762.1:p.=
XM_011522461.1:c.415-38137G>A XP_011520763.1:p.=
XM_011522458.3:c.-57-38137G>A XP_011520760.1:p.=
XM_011522461.3:c.415-38137G>A XP_011520763.1:p.=
XM_017023172.1:c.571-38137G>A XP_016878661.1:p.=
XM_017023173.1:c.571-38137G>A XP_016878662.1:p.=
NM_001134407.3:c.415-38137G>A MANE Select NP_001127879.1:p.=
NM_000833.5:c.415-38137G>A NP_000824.1:p.=