LDH info

Canonical Allele Identifier: CA14974927
Gene: DEPDC5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1012068

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.31869917T>G , CM000684.2:g.31869917T>G GRCh38
NC_000022.10:g.32265903T>G , CM000684.1:g.32265903T>G GRCh37
NC_000022.9:g.30595903T>G NCBI36
NG_034067.1:g.120967T>G

Transcript Alleles

HGVS Amino-acid change
NM_001136029.2:c.3304-673T>G VV NP_001129501.1:p.=
NM_001242896.1:c.3331-673T>G VV NP_001229825.1:p.=
NM_001242897.1:c.3031-673T>G VV NP_001229826.1:p.=
NM_014662.4:c.3238-673T>G VV NP_055477.1:p.=
NR_110988.1:n.3233-673T>G
XM_005261862.1:c.3331-673T>G XP_005261919.1:p.=
XM_011530557.1:c.3304-673T>G XP_011528859.1:p.=
XM_011530558.1:c.3265-673T>G XP_011528860.1:p.=
XM_011530559.1:c.3238-673T>G XP_011528861.1:p.=
XM_011530560.1:c.3097-673T>G XP_011528862.1:p.=
XM_011530561.1:c.3070-673T>G XP_011528863.1:p.=
XM_011530562.1:c.3331-673T>G XP_011528864.1:p.=
XM_011530563.1:c.3031-673T>G XP_011528865.1:p.=
XM_011530564.1:c.3331-673T>G XP_011528866.1:p.=
XM_011530565.1:c.3331-673T>G XP_011528867.1:p.=
XM_011530566.1:c.3331-673T>G XP_011528868.1:p.=
XM_011530567.1:c.3331-673T>G XP_011528869.1:p.=
XM_011530568.1:c.3265-673T>G XP_011528870.1:p.=
XM_011530569.1:c.1225-673T>G XP_011528871.1:p.=
XR_937972.1:n.3528-673T>G
XR_937973.1:n.3294-673T>G
NM_001136029.3:c.3304-673T>G VV NP_001129501.1:p.=
NM_001242896.2:c.3331-673T>G VV NP_001229825.1:p.=
NM_001363852.1:c.3265-673T>G VV NP_001350781.1:p.=
NM_001363854.1:c.3097-673T>G VV NP_001350783.1:p.=
NM_001364318.1:c.3331-673T>G VV NP_001351247.1:p.=
NM_001364319.1:c.3097-673T>G VV NP_001351248.1:p.=
NM_001364320.1:c.3265-673T>G VV NP_001351249.1:p.=
NM_014662.5:c.3238-673T>G VV NP_055477.1:p.=
NR_110988.2:n.3237-673T>G
NR_146296.1:n.3437-673T>G
NR_157125.1:n.3228-673T>G
NR_157126.1:n.3420-673T>G
NR_157128.1:n.3471-673T>G
XM_011530557.2:c.3304-673T>G XP_011528859.1:p.=
XM_011530559.2:c.3238-673T>G XP_011528861.1:p.=
XM_011530561.2:c.3070-673T>G XP_011528863.1:p.=
XM_011530562.2:c.3331-673T>G XP_011528864.1:p.=
XM_011530563.2:c.3031-673T>G XP_011528865.1:p.=
XM_011530565.2:c.3331-673T>G XP_011528867.1:p.=
XM_011530568.2:c.3265-673T>G XP_011528870.1:p.=
XM_011530569.2:c.1225-673T>G XP_011528871.1:p.=
XM_024452305.1:c.1198-673T>G XP_024308073.1:p.=
XR_001755389.1:n.3540-673T>G
XR_001755390.1:n.3540-673T>G
XR_937973.2:n.3306-673T>G
ENST00000382111.6:c.3331-673T>G ENSP00000371545.2:p.=
ENST00000382112.7:c.3304-673T>G ENSP00000371546.3:p.=
ENST00000400246.5:c.3331-673T>G ENSP00000383105.2:p.=
ENST00000400248.6:c.3238-673T>G ENSP00000383107.1:p.=
ENST00000400249.6:c.3238-673T>G ENSP00000383108.2:p.=
ENST00000433147.1:n.1457-673T>G
ENST00000448753.5:n.1387-673T>G ENSP00000402173.1:p.=
ENST00000494060.1:n.139-673T>G
ENST00000535622.5:c.3031-673T>G ENSP00000440210.1:p.=