LDH info

Canonical Allele Identifier: CA16479685
Gene: NALCN HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7988100

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101227208G>A , CM000675.2:g.101227208G>A GRCh38
NC_000013.10:g.101879559G>A , CM000675.1:g.101879559G>A GRCh37
NC_000013.9:g.100677560G>A NCBI36
NG_053176.1:g.194999C>T

Transcript Alleles

HGVS Amino-acid change
NM_052867.2:c.1626+2185C>T VV NP_443099.1:p.=
XM_011521067.1:c.1683+2185C>T XP_011519369.1:p.=
XM_011521068.1:c.1626+2185C>T XP_011519370.1:p.=
XM_011521069.1:c.1596+2185C>T XP_011519371.1:p.=
XM_011521070.1:c.1683+2185C>T XP_011519372.1:p.=
NM_001350748.1:c.1626+2185C>T VV NP_001337677.1:p.=
NM_001350749.1:c.1626+2185C>T VV NP_001337678.1:p.=
NM_001350750.1:c.1539+2185C>T VV NP_001337679.1:p.=
NM_001350751.1:c.1539+2185C>T VV NP_001337680.1:p.=
NM_052867.3:c.1626+2185C>T VV NP_443099.1:p.=
XM_011521067.2:c.1683+2185C>T XP_011519369.1:p.=
XM_011521069.2:c.1596+2185C>T XP_011519371.1:p.=
XM_017020536.2:c.1179+2185C>T XP_016876025.1:p.=
XM_017020537.1:c.861+2185C>T XP_016876026.1:p.=
XM_024449336.1:c.1683+2185C>T XP_024305104.1:p.=
NM_052867.4:c.1626+2185C>T VV MANE Preferred NP_443099.1:p.=
ENST00000251127.10:c.1626+2185C>T ENSP00000251127.6:p.=
ENST00000470333.1:n.1722+2185C>T
ENST00000497170.5:n.1780+2185C>T