LDH info

Canonical Allele Identifier: CA11952024
Gene: WWC1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10038727

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168459532G>A , CM000667.2:g.168459532G>A GRCh38
NC_000005.9:g.167886537G>A , CM000667.1:g.167886537G>A GRCh37
NC_000005.8:g.167819115G>A NCBI36
NG_016712.1:g.172473G>A

Transcript Alleles

HGVS Amino-acid change
NM_001161661.1:c.2824-1118G>A VV NP_001155133.1:p.=
NM_001161662.1:c.2824-1118G>A VV NP_001155134.1:p.=
NM_015238.2:c.2824-1118G>A VV NP_056053.1:p.=
XM_005265850.1:c.2839-1118G>A XP_005265907.1:p.=
XM_005265853.1:c.2824-1118G>A XP_005265910.1:p.=
XM_011534485.1:c.3022-1118G>A XP_011532787.1:p.=
XM_011534486.1:c.3022-1118G>A XP_011532788.1:p.=
XM_011534487.1:c.3007-1118G>A XP_011532789.1:p.=
XM_011534488.1:c.3022-1118G>A XP_011532790.1:p.=
XM_011534489.1:c.3007-1118G>A XP_011532791.1:p.=
XM_011534490.1:c.3022-1118G>A XP_011532792.1:p.=
XM_011534491.1:c.3007-1118G>A XP_011532793.1:p.=
XM_005265853.2:c.2824-1118G>A XP_005265910.1:p.=
XM_017009276.1:c.3007-1118G>A XP_016864765.1:p.=
XM_017009278.1:c.2557-1118G>A XP_016864767.1:p.=
NM_001161661.2:c.2824-1118G>A VV NP_001155133.1:p.=
NM_001161662.2:c.2824-1118G>A VV NP_001155134.1:p.=
NM_015238.3:c.2824-1118G>A VV MANE Preferred NP_056053.1:p.=
ENST00000265293.8:c.2824-1118G>A ENSP00000265293.4:p.=
ENST00000393895.7:n.2708-1118G>A
ENST00000521089.5:c.2824-1118G>A ENSP00000427772.1:p.=
ENST00000522140.1:n.640-1118G>A
ENST00000524038.5:n.802-1118G>A ENSP00000428084.1:p.=
ENST00000524228.5:n.2153-1118G>A
ENST00000619752.1:n.640-1118G>A ENSP00000483898.1:p.=