LDH info

Canonical Allele Identifier: CA16070360
Gene: DNM3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1011731

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172377408G>A , CM000663.2:g.172377408G>A GRCh38
NC_000001.10:g.172346548G>A , CM000663.1:g.172346548G>A GRCh37
NC_000001.9:g.170613171G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001136127.2:c.1882-1610G>A VV NP_001129599.1:p.=
NM_015569.4:c.1894-1610G>A VV NP_056384.2:p.=
XM_005245079.1:c.1924-1610G>A XP_005245136.1:p.=
XM_005245080.1:c.1912-1610G>A XP_005245137.1:p.=
XM_005245081.1:c.1924-1610G>A XP_005245138.1:p.=
XM_005245082.3:c.1594-1610G>A XP_005245139.1:p.=
XM_011509400.1:c.1924-1610G>A XP_011507702.1:p.=
XM_011509401.1:c.1924-1610G>A XP_011507703.1:p.=
XR_426865.1:n.32-772C>T
NM_001350204.1:c.1912-1610G>A VV NP_001337133.1:p.=
NM_001350206.1:c.1912-1610G>A VV NP_001337135.1:p.=
NR_146559.1:n.2107-1610G>A
XM_017000976.1:c.2068-1610G>A XP_016856465.1:p.=
XM_017000977.1:c.2056-1610G>A XP_016856466.1:p.=
XM_017000978.1:c.2038-1610G>A XP_016856467.1:p.=
XM_017000979.1:c.2068-1610G>A XP_016856468.1:p.=
XM_017000980.1:c.1939-1610G>A XP_016856469.1:p.=
XM_017000982.2:c.1912-1610G>A XP_016856471.1:p.=
XM_017000983.1:c.1894-1610G>A XP_016856472.1:p.=
XM_017000984.1:c.1882-1610G>A XP_016856473.1:p.=
XM_017000985.1:c.1882-1610G>A XP_016856474.1:p.=
XM_017000986.1:c.1783-1610G>A XP_016856475.1:p.=
XM_017000987.1:c.1594-1610G>A XP_016856476.1:p.=
XR_001737107.1:n.1964-1610G>A
XR_001737108.1:n.2102-1610G>A
XR_001737110.1:n.1946-1610G>A
XR_001737111.1:n.1814-1610G>A
NM_015569.5:c.1894-1610G>A VV MANE Preferred NP_056384.2:p.=
ENST00000355305.9:c.1912-1610G>A ENSP00000347457.5:p.=
ENST00000367731.5:c.1882-1610G>A ENSP00000356705.1:p.=
ENST00000465374.1:n.165-772C>T
ENST00000489002.5:n.259+723C>T
ENST00000627582.2:c.1894-1610G>A ENSP00000486701.1:p.=