LDH info

Canonical Allele Identifier: CA14569086
Gene: IMPA2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1020294

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12017344A>G , CM000680.2:g.12017344A>G GRCh38
NC_000018.9:g.12017343A>G , CM000680.1:g.12017343A>G GRCh37
NC_000018.8:g.12007343A>G NCBI36
NG_028104.1:g.40889A>G

Transcript Alleles

HGVS Amino-acid change
NM_014214.2:c.490+2971A>G VV NP_055029.1:p.=
XM_011525659.1:c.442+2971A>G XP_011523961.1:p.=
XM_011525660.1:c.418+2971A>G XP_011523962.1:p.=
XM_011525661.1:c.130+2971A>G XP_011523963.1:p.=
XM_011525659.3:c.442+2971A>G XP_011523961.1:p.=
XM_011525661.3:c.130+2971A>G XP_011523963.1:p.=
NM_014214.3:c.490+2971A>G VV MANE Preferred NP_055029.1:p.=
ENST00000269159.7:c.490+2971A>G ENSP00000269159.3:p.=
ENST00000383376.9:c.*492-270A>G ENSP00000372867.4:p.=
ENST00000586230.1:n.212+2971A>G
ENST00000588167.1:n.243+2971A>G
ENST00000588752.5:n.575+2971A>G
ENST00000588927.5:c.-78+2971A>G ENSP00000464767.1:p.=
ENST00000589238.5:c.-78+2971A>G ENSP00000465416.1:p.=
ENST00000590107.5:c.*132+2971A>G ENSP00000466059.1:p.=
ENST00000590138.1:c.*93+2971A>G ENSP00000465938.1:p.=