LDH info

Canonical Allele Identifier: CA15372969
Gene: GRIA1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10065813

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.153560845C>T , CM000667.2:g.153560845C>T GRCh38
NC_000005.9:g.152940405C>T , CM000667.1:g.152940405C>T GRCh37
NC_000005.8:g.152920598C>T NCBI36
NG_047078.1:g.76150C>T

Transcript Alleles

HGVS Amino-acid change
NM_000827.3:c.220+66780C>T VV NP_000818.2:p.=
NM_001114183.1:c.220+66780C>T VV NP_001107655.1:p.=
NM_001258019.1:c.220+66780C>T VV NP_001244948.1:p.=
NM_001258020.1:c.-66+51039C>T VV NP_001244949.1:p.=
NM_001258021.1:c.250+66780C>T VV NP_001244950.1:p.=
NM_001258022.1:c.250+66780C>T VV NP_001244951.1:p.=
NM_001258023.1:c.13+66780C>T VV NP_001244952.1:p.=
NR_047578.1:n.447+69875C>T
XM_011537635.1:c.160+66780C>T XP_011535937.1:p.=
XR_427776.2:n.490+66780C>T
NM_001364165.1:c.220+66780C>T VV NP_001351094.1:p.=
NM_001364166.1:c.247+66780C>T VV NP_001351095.1:p.=
NM_001364167.1:c.13+66780C>T VV NP_001351096.1:p.=
NR_157093.1:n.439+66780C>T
XM_017009392.1:c.250+66780C>T XP_016864881.1:p.=
NM_000827.4:c.220+66780C>T VV MANE Preferred NP_000818.2:p.=
ENST00000285900.9:c.220+66780C>T ENSP00000285900.4:p.=
ENST00000340592.9:c.220+66780C>T ENSP00000339343.5:p.=
ENST00000448073.8:c.250+66780C>T ENSP00000415569.2:p.=
ENST00000481559.6:n.361+66780C>T
ENST00000518142.5:c.220+66780C>T ENSP00000427920.1:p.=
ENST00000518783.1:c.250+66780C>T ENSP00000428994.1:p.=
ENST00000518862.5:n.168+66780C>T
ENST00000521843.6:c.13+66780C>T ENSP00000427864.2:p.=