Canonical Allele Identifier: CA277538505
Gene: GRIN2A HGNC NCBI

Linked Data

dbSNP Id: rs540019898
gnomAD v3: 16-9764743-A-T
gnomAD v4: 16-9764743-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764743A>T , CM000678.2:g.9764743A>T GRCh38
NC_000016.9:g.9858600A>T , CM000678.1:g.9858600A>T GRCh37
NC_000016.8:g.9766101A>T NCBI36
NG_011812.1:g.423012T>A
NG_011812.2:g.423012T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000330684.4:c.2801T>A MANE Select ENSP00000332549.3:p.Met934Lys
ENST00000535259.6:c.2330T>A ENSP00000441572.3:p.Met777Lys
ENST00000636273.2:n.2394T>A
ENST00000674742.1:c.2330T>A ENSP00000502200.1:p.Met777Lys
ENST00000675398.1:c.*171T>A ENSP00000502752.1:n.*171T>A
ENST00000330684.3:c.2801T>A ENSP00000332549.3:p.Met934Lys
ENST00000396573.6:c.2801T>A ENSP00000379818.2:p.Met934Lys
ENST00000396575.6:c.2390T>A ENSP00000379820.3:p.Met797Lys
ENST00000461292.3:n.2440T>A
ENST00000535259.5:c.2390T>A ENSP00000441572.2:p.Met797Lys
ENST00000562109.5:c.2801T>A ENSP00000454998.1:p.Met934Lys
NM_000833.4:c.2801T>A NP_000824.1:p.Met934Lys
NM_001134407.2:c.2801T>A NP_001127879.1:p.Met934Lys
NM_001134408.2:c.2801T>A NP_001127880.1:p.Met934Lys
XM_011522456.1:c.2642T>A XP_011520758.1:p.Met881Lys
XM_011522457.1:c.2543T>A XP_011520759.1:p.Met848Lys
XM_011522458.1:c.2330T>A XP_011520760.1:p.Met777Lys
XM_011522459.1:c.2330T>A XP_011520761.1:p.Met777Lys
XM_011522460.1:c.2330T>A XP_011520762.1:p.Met777Lys
XM_011522461.1:c.2801T>A XP_011520763.1:p.Met934Lys
XM_011522458.3:c.2330T>A XP_011520760.1:p.Met777Lys
XM_011522461.3:c.2801T>A XP_011520763.1:p.Met934Lys
XM_017023172.1:c.2957T>A XP_016878661.1:p.Met986Lys
XM_017023173.1:c.2957T>A XP_016878662.1:p.Met986Lys
NM_001134407.3:c.2801T>A MANE Select NP_001127879.1:p.Met934Lys
NM_000833.5:c.2801T>A NP_000824.1:p.Met934Lys