LDH info

Canonical Allele Identifier: CA314972
Gene: GRIN2A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs796052556

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9764203C>G , CM000678.2:g.9764203C>G GRCh38
NC_000016.9:g.9858060C>G , CM000678.1:g.9858060C>G GRCh37
NC_000016.8:g.9765561C>G NCBI36
NG_011812.1:g.423552G>C
NG_011812.2:g.423552G>C

Transcript Alleles

HGVS Amino-acid change
NM_000833.4:c.3341G>C VV NP_000824.1:p.Arg1114Thr
NM_001134407.2:c.3341G>C VV NP_001127879.1:p.Arg1114Thr
NM_001134408.2:c.3341G>C VV NP_001127880.1:p.Arg1114Thr
XM_011522456.1:c.3182G>C XP_011520758.1:p.Arg1061Thr
XM_011522457.1:c.3083G>C XP_011520759.1:p.Arg1028Thr
XM_011522458.1:c.2870G>C XP_011520760.1:p.Arg957Thr
XM_011522459.1:c.2870G>C XP_011520761.1:p.Arg957Thr
XM_011522460.1:c.2870G>C XP_011520762.1:p.Arg957Thr
XM_011522461.1:c.3341G>C XP_011520763.1:p.Arg1114Thr
XM_011522458.3:c.2870G>C XP_011520760.1:p.Arg957Thr
XM_011522461.3:c.3341G>C XP_011520763.1:p.Arg1114Thr
XM_017023172.1:c.3497G>C XP_016878661.1:p.Arg1166Thr
XM_017023173.1:c.3497G>C XP_016878662.1:p.Arg1166Thr
NM_001134407.3:c.3341G>C VV MANE Preferred NP_001127879.1:p.Arg1114Thr
NM_000833.5:c.3341G>C VV NP_000824.1:p.Arg1114Thr
ENST00000330684.3:c.3341G>C ENSP00000332549.3:p.Arg1114Thr
ENST00000396573.6:c.3341G>C ENSP00000379818.2:p.Arg1114Thr
ENST00000396575.6:n.2930G>C ENSP00000379820.3:p.Arg977Thr
ENST00000461292.3:n.2980G>C
ENST00000535259.5:c.2930G>C ENSP00000441572.2:p.Arg977Thr
ENST00000562109.5:c.3341G>C ENSP00000454998.1:p.Arg1114Thr