LDH info

Canonical Allele Identifier: CA123383
Gene: PRF1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13709
dbSNP Id: rs104894176

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598599C>T , CM000672.2:g.70598599C>T GRCh38
NC_000010.10:g.72358355C>T , CM000672.1:g.72358355C>T GRCh37
NC_000010.9:g.72028361C>T NCBI36
NG_009615.1:g.9177G>A , LRG_94:g.9177G>A

Transcript Alleles

HGVS Amino-acid change
NM_001083116.1:c.1122G>A , LRG_94t1:c.1122G>A NP_001076585.1:p.Trp374Ter
NM_005041.4:c.1122G>A VV NP_005032.2:p.Trp374Ter
NM_001083116.2:c.1122G>A VV NP_001076585.1:p.Trp374Ter
NM_005041.5:c.1122G>A VV NP_005032.2:p.Trp374Ter
NM_001083116.3:c.1122G>A VV MANE Preferred NP_001076585.1:p.Trp374Ter
ENST00000373209.2:c.1122G>A ENSP00000362305.1:p.Trp374Ter
ENST00000441259.1:c.1122G>A ENSP00000398568.1:p.Trp374Ter