LDH info

Canonical Allele Identifier: CA221968364
Gene: TSPAN18 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11038167

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44821583A>C , CM000673.2:g.44821583A>C GRCh38
NC_000011.9:g.44843134A>C , CM000673.1:g.44843134A>C GRCh37
NC_000011.8:g.44799710A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_130783.4:c.-152-38745A>C VV NP_570139.3:p.=
XM_005253217.2:c.-199-38745A>C XP_005253274.1:p.=
XM_006718372.2:c.-199-38745A>C XP_006718435.1:p.=
XM_006718373.2:c.-152-38745A>C XP_006718436.1:p.=
XM_011520459.1:c.-161-38745A>C XP_011518761.1:p.=
XM_005253217.3:c.-199-38745A>C XP_005253274.1:p.=
XM_006718372.3:c.-199-38745A>C XP_006718435.1:p.=
XM_006718373.4:c.-152-38745A>C XP_006718436.1:p.=
XM_011520459.3:c.-161-38745A>C XP_011518761.1:p.=
XM_017018530.1:c.-199-38745A>C XP_016874019.1:p.=
XM_017018531.1:c.-152-38745A>C XP_016874020.1:p.=
NM_130783.5:c.-152-38745A>C VV MANE Preferred NP_570139.3:p.=
ENST00000340160.7:c.-152-38745A>C ENSP00000339820.3:p.=
ENST00000520358.6:c.-152-38745A>C ENSP00000429993.2:p.=
ENST00000520999.6:c.-199-38745A>C ENSP00000427942.2:p.=
ENST00000533080.5:c.-152-38745A>C ENSP00000433362.1:p.=
ENST00000533202.5:c.-152-38745A>C ENSP00000434625.1:p.=
ENST00000533786.5:c.-152-38745A>C ENSP00000433592.1:p.=