LDH info

Canonical Allele Identifier: CA192412466
Gene: APTX HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17324756

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33014687T>C , CM000671.2:g.33014687T>C GRCh38
NC_000009.11:g.33014685T>C , CM000671.1:g.33014685T>C GRCh37
NC_000009.10:g.33004685T>C NCBI36
NG_012821.2:g.15445A>G

Transcript Alleles

HGVS Amino-acid change
XM_011517936.1:c.-264+10336A>G XP_011516238.1:p.=
XM_011517937.1:c.-222+10313A>G XP_011516239.1:p.=
XM_017014837.2:c.-5+10117A>G XP_016870326.1:p.=
XM_024447575.1:c.-5+10117A>G XP_024303343.1:p.=
XM_024447576.1:c.-5+10313A>G XP_024303344.1:p.=
XM_024447577.1:c.-5+10336A>G XP_024303345.1:p.=
XM_024447579.1:c.-5+10117A>G XP_024303347.1:p.=
XM_024447580.1:c.-5+10336A>G XP_024303348.1:p.=
XM_024447581.1:c.-264+10117A>G XP_024303349.1:p.=
XM_024447582.1:c.-264+10313A>G XP_024303350.1:p.=
NM_001368995.1:c.-5+10313A>G VV NP_001355924.1:p.=
NM_001368996.1:c.-5+10336A>G VV NP_001355925.1:p.=
NM_001368997.1:c.-5+10117A>G VV NP_001355926.1:p.=
NM_001368999.1:c.-5+10117A>G VV NP_001355928.1:p.=
NM_001369000.1:c.-5+10117A>G VV NP_001355929.1:p.=
NM_001369001.1:c.-5+10336A>G VV NP_001355930.1:p.=
NM_001369002.1:c.-264+10313A>G VV NP_001355931.1:p.=
NM_001369003.1:c.-264+10117A>G VV NP_001355932.1:p.=
NR_160922.1:n.317+10117A>G
NR_160923.1:n.121+10313A>G
NR_160924.1:n.121+10313A>G
NR_160925.1:n.317+10117A>G
NR_160926.1:n.121+10313A>G
NR_160927.1:n.317+10117A>G
NR_160928.1:n.317+10117A>G
NR_160929.1:n.121+10313A>G
ENST00000460945.5:n.169+10313A>G
ENST00000495360.5:c.-5+10117A>G ENSP00000419623.1:p.=