LDH info

Canonical Allele Identifier: CA15183814
Gene: PRKCE HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12373805

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46093955G>A , CM000664.2:g.46093955G>A GRCh38
NC_000002.11:g.46321094G>A , CM000664.1:g.46321094G>A GRCh37
NC_000002.10:g.46174598G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_005400.2:c.1592+7593G>A VV NP_005391.1:p.=
XM_005264428.1:c.1592+7593G>A XP_005264485.1:p.=
XM_005264429.1:c.1181+7593G>A XP_005264486.1:p.=
XM_006712050.2:c.761+7593G>A XP_006712113.1:p.=
XM_011532970.1:c.1304+7593G>A XP_011531272.1:p.=
XM_011532971.1:c.1304+7593G>A XP_011531273.1:p.=
XM_011532972.1:c.1304+7593G>A XP_011531274.1:p.=
XM_011532973.1:c.1304+7593G>A XP_011531275.1:p.=
XM_011532974.1:c.1304+7593G>A XP_011531276.1:p.=
XM_011532975.1:c.1304+7593G>A XP_011531277.1:p.=
XM_011532976.1:c.1304+7593G>A XP_011531278.1:p.=
XM_011532977.1:c.1250+7593G>A XP_011531279.1:p.=
XM_011532978.1:c.1250+7593G>A XP_011531280.1:p.=
XM_011532979.1:c.1247+7593G>A XP_011531281.1:p.=
XM_011532980.1:c.1142+7593G>A XP_011531282.1:p.=
XM_011532981.1:c.1142+7593G>A XP_011531283.1:p.=
XM_011532982.1:c.872+7593G>A XP_011531284.1:p.=
XM_011532983.1:c.689+7593G>A XP_011531285.1:p.=
XM_006712050.3:c.761+7593G>A XP_006712113.1:p.=
XM_011532971.3:c.1304+7593G>A XP_011531273.1:p.=
XM_011532975.3:c.1304+7593G>A XP_011531277.1:p.=
XM_011532978.2:c.1250+7593G>A XP_011531280.1:p.=
XM_011532980.3:c.1142+7593G>A XP_011531282.1:p.=
XM_011532981.3:c.1142+7593G>A XP_011531283.1:p.=
XM_011532982.2:c.872+7593G>A XP_011531284.1:p.=
XM_011532983.2:c.689+7593G>A XP_011531285.1:p.=
XM_017004486.2:c.1304+7593G>A XP_016859975.1:p.=
XM_017004487.2:c.1250+7593G>A XP_016859976.1:p.=
XM_017004488.2:c.1250+7593G>A XP_016859977.1:p.=
XM_017004489.2:c.1142+7593G>A XP_016859978.1:p.=
XM_017004490.2:c.1142+7593G>A XP_016859979.1:p.=
XM_017004491.2:c.1142+7593G>A XP_016859980.1:p.=
XM_024452991.1:c.1142+7593G>A XP_024308759.1:p.=
XM_024452992.1:c.1142+7593G>A XP_024308760.1:p.=
NM_005400.3:c.1592+7593G>A VV MANE Preferred NP_005391.1:p.=
ENST00000306156.7:c.1592+7593G>A ENSP00000306124.3:p.=
ENST00000469753.5:n.679+7593G>A
ENST00000480633.1:n.358+7593G>A