LDH info

Canonical Allele Identifier: CA145523
Gene: ADAM10 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 92164
ClinVar RCV Id: RCV000077798
dbSNP Id: rs145518263

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58665141T>C , CM000677.2:g.58665141T>C GRCh38
NC_000015.9:g.58957340T>C , CM000677.1:g.58957340T>C GRCh37
NC_000015.8:g.56744632T>C NCBI36
NG_033876.1:g.89838A>G

Transcript Alleles

HGVS Amino-acid change
NM_001110.3:c.541A>G VV NP_001101.1:p.Arg181Gly
XM_005254117.2:c.541A>G XP_005254174.1:p.Arg181Gly
NM_001320570.1:c.541A>G VV NP_001307499.1:p.Arg181Gly
XM_024449818.1:c.319A>G XP_024305586.1:p.Arg107Gly
NM_001110.4:c.541A>G VV MANE Preferred NP_001101.1:p.Arg181Gly
ENST00000260408.7:c.541A>G ENSP00000260408.3:p.Arg181Gly
ENST00000396136.6:n.367A>G
ENST00000402627.5:c.56-24311A>G ENSP00000386056.1:p.=
ENST00000558733.5:n.777A>G
ENST00000559053.1:c.56-24311A>G ENSP00000453952.1:p.=
ENST00000561288.1:c.56-67623A>G ENSP00000452639.1:p.=