LDH info

Canonical Allele Identifier: CA14959758
Gene: CSNK1E HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1534891

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.38299094T>C , CM000684.2:g.38299094T>C GRCh38
NC_000022.10:g.38695099T>C , CM000684.1:g.38695099T>C GRCh37
NC_000022.9:g.37025045T>C NCBI36
NG_016707.1:g.23991A>G

Transcript Alleles

HGVS Amino-acid change
NM_001289912.1:c.737-160A>G VV NP_001276841.1:p.=
NM_001894.4:c.737-160A>G VV NP_001885.1:p.=
NM_152221.2:c.737-160A>G VV NP_689407.1:p.=
NM_152221.3:c.737-160A>G VV MANE Preferred NP_689407.1:p.=
ENST00000359867.7:c.737-160A>G ENSP00000352929.3:p.=
ENST00000396832.5:c.737-160A>G ENSP00000380044.1:p.=
ENST00000400206.6:c.737-160A>G ENSP00000383067.2:p.=
ENST00000403904.5:c.737-160A>G ENSP00000384074.1:p.=
ENST00000405675.7:c.737-160A>G ENSP00000384426.3:p.=
ENST00000413574.6:c.737-160A>G ENSP00000407235.2:p.=
ENST00000431611.5:n.212-160A>G
ENST00000442216.1:n.132-160A>G
ENST00000451964.5:n.550-160A>G
ENST00000498529.5:n.172-160A>G
ENST00000612795.1:n.531-160A>G