LDH info

Canonical Allele Identifier: CA13496826
Gene: PAMR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10768140

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35489359T>G , CM000673.2:g.35489359T>G GRCh38
NC_000011.9:g.35510907T>G , CM000673.1:g.35510907T>G GRCh37
NC_000011.8:g.35467483T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001001991.2:c.379+2686A>C VV NP_001001991.1:p.=
NM_001282675.1:c.259+2686A>C VV NP_001269604.1:p.=
NM_001282676.1:c.379+2686A>C VV NP_001269605.1:p.=
NM_015430.3:c.379+2686A>C VV NP_056245.2:p.=
ENST00000527605.5:c.259+2686A>C ENSP00000432591.1:p.=
ENST00000529303.1:c.379+2686A>C ENSP00000433024.1:p.=
ENST00000534803.1:n.391+2686A>C
ENST00000611014.4:c.-532+2686A>C ENSP00000478867.1:p.=
ENST00000615849.4:c.379+2686A>C ENSP00000479260.1:p.=
ENST00000619888.4:c.379+2686A>C ENSP00000483703.1:p.=
ENST00000621476.4:c.259+2686A>C ENSP00000480961.1:p.=
ENST00000622144.4:c.379+2686A>C ENSP00000482899.1:p.=