LDH info

Canonical Allele Identifier: CA13851351
Gene: NALCN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs582504

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101060982G>T , CM000675.2:g.101060982G>T GRCh38
NC_000013.10:g.101713334G>T , CM000675.1:g.101713334G>T GRCh37
NC_000013.9:g.100511335G>T NCBI36
NG_053176.1:g.361225C>A

Transcript Alleles

HGVS Amino-acid change
NM_052867.2:c.4755+986C>A VV NP_443099.1:p.=
XM_011521067.1:c.4812+986C>A XP_011519369.1:p.=
XM_011521068.1:c.4755+986C>A XP_011519370.1:p.=
XM_011521069.1:c.4725+986C>A XP_011519371.1:p.=
XM_011521070.1:c.4533+986C>A XP_011519372.1:p.=
NM_001350748.1:c.4842+986C>A VV NP_001337677.1:p.=
NM_001350749.1:c.4755+986C>A VV NP_001337678.1:p.=
NM_001350750.1:c.4668+986C>A VV NP_001337679.1:p.=
NM_001350751.1:c.4668+986C>A VV NP_001337680.1:p.=
NM_052867.3:c.4755+986C>A VV NP_443099.1:p.=
XM_011521067.2:c.4812+986C>A XP_011519369.1:p.=
XM_011521069.2:c.4725+986C>A XP_011519371.1:p.=
XM_017020536.2:c.4308+986C>A XP_016876025.1:p.=
XM_017020537.1:c.3990+986C>A XP_016876026.1:p.=
XM_024449336.1:c.4899+986C>A XP_024305104.1:p.=
NM_052867.4:c.4755+986C>A VV MANE Preferred NP_443099.1:p.=
ENST00000251127.10:c.4755+986C>A ENSP00000251127.6:p.=