LDH info

Canonical Allele Identifier: CA126953
Gene: CYP2D6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16891
dbSNP Id: rs5030655

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42129084del , CM000684.2:g.42129084del GRCh38
NC_000022.10:g.42525086del , CM000684.1:g.42525086del GRCh37
NC_000022.9:g.40855030del NCBI36
NG_008376.3:g.5908del
NG_008376.4:g.6727del

Transcript Alleles

HGVS Amino-acid change
NM_000106.5:c.454del VV NP_000097.3:p.Trp152GlyfsTer2
NM_001025161.2:c.353-140del VV NP_001020332.2:p.=
XM_011529966.1:c.454del XP_011528268.1:p.Trp152GlyfsTer2
XM_011529967.1:c.454del XP_011528269.1:p.Trp152GlyfsTer2
XM_011529968.1:c.454del XP_011528270.1:p.Trp152GlyfsTer2
XM_011529969.1:c.311del XP_011528271.1:p.Val104GlyfsTer?
XM_011529970.1:c.353-140del XP_011528272.1:p.=
XM_011529971.1:c.311del XP_011528273.1:p.Val104GlyfsTer?
XM_011529972.1:c.454del XP_011528274.1:p.Trp152GlyfsTer2
NM_000106.6:c.454del VV NP_000097.3:p.Trp152GlyfsTer2
ENST00000359033.4:c.353-140del ENSP00000351927.4:p.=
ENST00000360124.9:n.173-140del ENSP00000353241.5:p.=
ENST00000360608.9:c.454del ENSP00000353820.5:p.Trp152GlyfsTer2
ENST00000389970.7:c.388del ENSP00000374620.4:p.Trp130GlyfsTer2
ENST00000488442.1:n.1178del