Canonical Allele Identifier: CA394798452
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938157T>C , CM000678.2:g.9938157T>C GRCh38
NC_000016.9:g.10032014T>C , CM000678.1:g.10032014T>C GRCh37
NC_000016.8:g.9939515T>C NCBI36
NG_011812.1:g.249598A>G
NG_011812.2:g.249598A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330684.4:c.809A>G MANE Select ENSP00000332549.3:p.Lys270Arg
ENST00000535259.6:c.338A>G ENSP00000441572.3:p.Lys113Arg
ENST00000636273.2:n.402A>G
ENST00000637393.1:c.401A>G ENSP00000490232.1:p.Lys134Arg
ENST00000674742.1:c.338A>G ENSP00000502200.1:p.Lys113Arg
ENST00000675189.1:n.1293A>G
ENST00000675398.1:c.809A>G ENSP00000502752.1:p.Lys270Arg
ENST00000330684.3:c.809A>G ENSP00000332549.3:p.Lys270Arg
ENST00000396573.6:c.809A>G ENSP00000379818.2:p.Lys270Arg
ENST00000396575.6:c.398A>G ENSP00000379820.3:p.Lys133Arg
ENST00000461292.3:n.448A>G
ENST00000535259.5:c.398A>G ENSP00000441572.2:p.Lys133Arg
ENST00000562109.5:c.809A>G ENSP00000454998.1:p.Lys270Arg
ENST00000566670.2:n.651A>G
ENST00000566683.1:n.241-47057A>G
ENST00000568247.3:n.701A>G
NM_000833.4:c.809A>G NP_000824.1:p.Lys270Arg
NM_001134407.2:c.809A>G NP_001127879.1:p.Lys270Arg
NM_001134408.2:c.809A>G NP_001127880.1:p.Lys270Arg
XM_011522456.1:c.650A>G XP_011520758.1:p.Lys217Arg
XM_011522457.1:c.551A>G XP_011520759.1:p.Lys184Arg
XM_011522458.1:c.338A>G XP_011520760.1:p.Lys113Arg
XM_011522459.1:c.338A>G XP_011520761.1:p.Lys113Arg
XM_011522460.1:c.338A>G XP_011520762.1:p.Lys113Arg
XM_011522461.1:c.809A>G XP_011520763.1:p.Lys270Arg
XM_011522458.3:c.338A>G XP_011520760.1:p.Lys113Arg
XM_011522461.3:c.809A>G XP_011520763.1:p.Lys270Arg
XM_017023172.1:c.965A>G XP_016878661.1:p.Lys322Arg
XM_017023173.1:c.965A>G XP_016878662.1:p.Lys322Arg
NM_001134407.3:c.809A>G MANE Select NP_001127879.1:p.Lys270Arg
NM_000833.5:c.809A>G NP_000824.1:p.Lys270Arg