LDH info

Canonical Allele Identifier: CA261175
Gene: ADAMTSL4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 39554
ClinVar RCV Id: RCV000032752
dbSNP Id: rs587776927

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150552897G>A , CM000663.2:g.150552897G>A GRCh38
NC_000001.10:g.150525373G>A , CM000663.1:g.150525373G>A GRCh37
NC_000001.9:g.148791997G>A NCBI36
NG_012172.1:g.8476G>A

Transcript Alleles

HGVS Amino-acid change
NM_001288607.1:c.79-1G>A VV NP_001275536.1:p.=
NM_001288608.1:c.79-1G>A VV NP_001275537.1:p.=
NM_019032.5:c.79-1G>A VV NP_061905.2:p.=
NM_025008.4:c.79-1G>A VV NP_079284.2:p.=
XM_011509644.1:c.178-1G>A XP_011507946.1:p.=
XM_011509645.1:c.178-1G>A XP_011507947.1:p.=
XM_011509646.1:c.79-1G>A XP_011507948.1:p.=
XM_011509647.1:c.79-1G>A XP_011507949.1:p.=
XM_011509648.1:c.79-1G>A XP_011507950.1:p.=
XM_011509649.1:c.178-1G>A XP_011507951.1:p.=
XM_011509650.1:c.178-1G>A XP_011507952.1:p.=
XR_921844.1:n.363-1G>A
XR_922132.1:n.370+1638C>T
XR_922133.1:n.417+1638C>T
XM_011509644.3:c.178-1G>A XP_011507946.1:p.=
XM_011509645.3:c.178-1G>A XP_011507947.1:p.=
XM_011509648.3:c.79-1G>A XP_011507950.1:p.=
XM_011509649.3:c.178-1G>A XP_011507951.1:p.=
XM_011509650.3:c.178-1G>A XP_011507952.1:p.=
XM_017001506.2:c.79-1G>A XP_016856995.1:p.=
XR_001737242.2:n.336-1G>A
XR_001738226.1:n.495C>T
XR_001738227.1:n.466+1638C>T
XR_001738228.1:n.400C>T
XR_001738229.1:n.357+3057C>T
XR_921844.3:n.336-1G>A
NM_001288607.2:c.79-1G>A VV NP_001275536.1:p.=
NM_025008.5:c.79-1G>A VV NP_079284.2:p.=
ENST00000271643.8:c.79-1G>A ENSP00000271643.4:p.=
ENST00000369038.6:c.79-1G>A ENSP00000358034.2:p.=
ENST00000369039.9:c.79-1G>A ENSP00000358035.5:p.=
ENST00000369041.9:c.79-1G>A ENSP00000358037.5:p.=