LDH info

Canonical Allele Identifier: CA12159028
Gene: COMMD10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10043228

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.116261351C>T , CM000667.2:g.116261351C>T GRCh38
NC_000005.9:g.115597048C>T , CM000667.1:g.115597048C>T GRCh37
NC_000005.8:g.115624947C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001308080.1:c.469-30166C>T VV NP_001295009.1:p.=
NM_016144.2:c.511-30166C>T VV NP_057228.1:p.=
NM_016144.3:c.511-30166C>T VV NP_057228.1:p.=
XR_948268.1:n.564-30166C>T
XR_948269.1:n.564-30166C>T
XR_948270.1:n.564-30166C>T
XR_948271.1:n.564-30166C>T
XM_017009553.1:c.469-30166C>T XP_016865042.1:p.=
XR_001742095.2:n.564-30166C>T
XR_001742096.2:n.564-30166C>T
XR_001742097.1:n.564-30166C>T
XR_001742098.1:n.564-30166C>T
XR_001742099.2:n.564-30166C>T
XR_001742100.1:n.564-30166C>T
XR_001742101.1:n.564-30166C>T
XR_002956162.1:n.564-30166C>T
XR_948270.2:n.564-30166C>T
NM_016144.4:c.511-30166C>T VV MANE Preferred NP_057228.1:p.=
ENST00000274458.8:c.511-30166C>T ENSP00000274458.4:p.=
ENST00000506589.1:n.268-30166C>T ENSP00000424611.1:p.=
ENST00000507356.5:c.*86-30166C>T ENSP00000422448.1:p.=
ENST00000515539.5:c.469-30166C>T ENSP00000427319.1:p.=
ENST00000632434.1:c.469-30166C>T ENSP00000488332.1:p.=