Canonical Allele Identifier: CA394798648
Gene: GRIN2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9938247A>C , CM000678.2:g.9938247A>C GRCh38
NC_000016.9:g.10032104A>C , CM000678.1:g.10032104A>C GRCh37
NC_000016.8:g.9939605A>C NCBI36
NG_011812.1:g.249508T>G
NG_011812.2:g.249508T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.719T>G MANE Select ENSP00000332549.3:p.Leu240Arg
ENST00000535259.6:c.248T>G ENSP00000441572.3:p.Leu83Arg
ENST00000636273.2:n.312T>G
ENST00000637393.1:c.311T>G ENSP00000490232.1:p.Leu104Arg
ENST00000674742.1:c.248T>G ENSP00000502200.1:p.Leu83Arg
ENST00000675189.1:n.1203T>G
ENST00000675398.1:c.719T>G ENSP00000502752.1:p.Leu240Arg
ENST00000330684.3:c.719T>G ENSP00000332549.3:p.Leu240Arg
ENST00000396573.6:c.719T>G ENSP00000379818.2:p.Leu240Arg
ENST00000396575.6:c.308T>G ENSP00000379820.3:p.Leu103Arg
ENST00000461292.3:n.358T>G
ENST00000535259.5:c.308T>G ENSP00000441572.2:p.Leu103Arg
ENST00000562109.5:c.719T>G ENSP00000454998.1:p.Leu240Arg
ENST00000566670.2:n.561T>G
ENST00000566683.1:n.241-47147T>G
ENST00000568247.3:n.611T>G
NM_000833.4:c.719T>G NP_000824.1:p.Leu240Arg
NM_001134407.2:c.719T>G NP_001127879.1:p.Leu240Arg
NM_001134408.2:c.719T>G NP_001127880.1:p.Leu240Arg
XM_011522456.1:c.560T>G XP_011520758.1:p.Leu187Arg
XM_011522457.1:c.461T>G XP_011520759.1:p.Leu154Arg
XM_011522458.1:c.248T>G XP_011520760.1:p.Leu83Arg
XM_011522459.1:c.248T>G XP_011520761.1:p.Leu83Arg
XM_011522460.1:c.248T>G XP_011520762.1:p.Leu83Arg
XM_011522461.1:c.719T>G XP_011520763.1:p.Leu240Arg
XM_011522458.3:c.248T>G XP_011520760.1:p.Leu83Arg
XM_011522461.3:c.719T>G XP_011520763.1:p.Leu240Arg
XM_017023172.1:c.875T>G XP_016878661.1:p.Leu292Arg
XM_017023173.1:c.875T>G XP_016878662.1:p.Leu292Arg
NM_001134407.3:c.719T>G MANE Select NP_001127879.1:p.Leu240Arg
NM_000833.5:c.719T>G NP_000824.1:p.Leu240Arg