LDH info

Canonical Allele Identifier: CA341153
Gene: PRSS1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11878
ClinVar RCV Id: RCV000012653
dbSNP Id: rs111033567

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.142750582A>G , CM000669.2:g.142750582A>G GRCh38
NC_000007.13:g.142458433A>G , CM000669.1:g.142458433A>G GRCh37
NC_000007.12:g.142138007A>G NCBI36
NG_008307.3:g.6099A>G

Transcript Alleles

HGVS Amino-acid change
NM_002769.4:c.68A>G VV NP_002760.1:p.Lys23Arg
XM_011516411.1:c.743A>G XP_011514713.1:p.Lys248Arg
NM_002769.5:c.68A>G VV MANE Preferred NP_002760.1:p.Lys23Arg
ENST00000311737.11:c.68A>G ENSP00000308720.7:p.Lys23Arg
ENST00000485223.1:n.54-47A>G
ENST00000486171.5:c.68A>G ENSP00000417854.1:p.Lys23Arg
ENST00000497041.1:n.72A>G
ENST00000610416.2:c.370+29396A>G ENSP00000482915.1:p.=
ENST00000612126.4:c.68A>G ENSP00000479959.1:p.Lys23Arg
ENST00000619214.4:c.68A>G ENSP00000481361.1:p.Lys23Arg
ENST00000633114.1:c.68A>G ENSP00000487822.1:p.Lys23Arg
ENST00000634019.1:c.82+1791A>G ENSP00000488594.1:p.=