LDH info

Canonical Allele Identifier: CA216844
Gene: KRT14 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 66313
ClinVar RCV Id: RCV000056676
dbSNP Id: rs267607400

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583281G>A , CM000679.2:g.41583281G>A GRCh38
NC_000017.10:g.39739533G>A , CM000679.1:g.39739533G>A GRCh37
NC_000017.9:g.36993059G>A NCBI36
NG_008624.1:g.8615C>T

Transcript Alleles

HGVS Amino-acid change
NM_000526.4:c.1228C>T VV NP_000517.2:p.Gln410Ter
NM_000526.5:c.1228C>T VV MANE Preferred NP_000517.3:p.Gln410Ter
ENST00000167586.6:c.1228C>T ENSP00000167586.6:p.Gln410Ter
ENST00000441550.2:n.175C>T
ENST00000476662.1:n.678C>T