LDH info

Canonical Allele Identifier: CA116465
Gene: LYST HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 3817
dbSNP Id: rs28942077

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235766204A>T , CM000663.2:g.235766204A>T GRCh38
NC_000001.10:g.235929504A>T , CM000663.1:g.235929504A>T GRCh37
NC_000001.9:g.233996127A>T NCBI36
NG_007397.1:g.122437T>A , LRG_143:g.122437T>A

Transcript Alleles

HGVS Amino-acid change
NM_000081.3:c.5996T>A , LRG_143t1:c.5996T>A NP_000072.2:p.Val1999Asp
NM_001301365.1:c.5996T>A , LRG_143t2:c.5996T>A NP_001288294.1:p.Val1999Asp
XM_011544031.1:c.5996T>A XP_011542333.1:p.Val1999Asp
XM_011544032.1:c.5996T>A XP_011542334.1:p.Val1999Asp
XM_011544033.1:c.5996T>A XP_011542335.1:p.Val1999Asp
XM_011544034.1:c.5858T>A XP_011542336.1:p.Val1953Asp
XM_011544035.1:c.5996T>A XP_011542337.1:p.Val1999Asp
XM_011544036.1:c.3659T>A XP_011542338.1:p.Val1220Asp
XM_011544037.1:c.5996T>A XP_011542339.1:p.Val1999Asp
XM_011544038.1:c.5996T>A XP_011542340.1:p.Val1999Asp
XM_011544039.1:c.5996T>A XP_011542341.1:p.Val1999Asp
XM_011544040.1:c.5961+35T>A XP_011542342.1:p.=
XM_011544033.2:c.5996T>A XP_011542335.1:p.Val1999Asp
XM_011544035.2:c.5996T>A XP_011542337.1:p.Val1999Asp
XM_011544036.2:c.3659T>A XP_011542338.1:p.Val1220Asp
XM_011544037.2:c.5996T>A XP_011542339.1:p.Val1999Asp
XM_011544039.2:c.5996T>A XP_011542341.1:p.Val1999Asp
XM_017000150.1:c.5996T>A XP_016855639.1:p.Val1999Asp
XM_017000151.1:c.5823+35T>A XP_016855640.1:p.=
XR_001736946.2:n.6178T>A
XR_001736947.1:n.6178T>A
XR_001736948.1:n.6178T>A
XR_002959252.1:n.6143+35T>A
ENST00000389793.6:c.5996T>A ENSP00000374443.2:p.Val1999Asp
ENST00000389794.7:c.*1420T>A ENSP00000374444.4:p.=
ENST00000489585.5:n.6512+35T>A