Canonical Allele Identifier: CA10581447
Gene: NALCN HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 235836
ClinVar RCV Id: RCV000224921
dbSNP Id: rs878853133

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101292058C>T , CM000675.2:g.101292058C>T GRCh38
NC_000013.10:g.101944409C>T , CM000675.1:g.101944409C>T GRCh37
NC_000013.9:g.100742410C>T NCBI36
NG_053176.1:g.130149G>A

Transcript Alleles

HGVS Amino-acid change
NM_052867.2:c.979G>A VV NP_443099.1:p.Glu327Lys
XM_011521067.1:c.1036G>A XP_011519369.1:p.Glu346Lys
XM_011521068.1:c.979G>A XP_011519370.1:p.Glu327Lys
XM_011521069.1:c.1036G>A XP_011519371.1:p.Glu346Lys
XM_011521070.1:c.1036G>A XP_011519372.1:p.Glu346Lys
NM_001350748.1:c.979G>A VV NP_001337677.1:p.Glu327Lys
NM_001350749.1:c.979G>A VV NP_001337678.1:p.Glu327Lys
NM_001350750.1:c.979G>A VV NP_001337679.1:p.Glu327Lys
NM_001350751.1:c.979G>A VV NP_001337680.1:p.Glu327Lys
NM_052867.3:c.979G>A VV NP_443099.1:p.Glu327Lys
XM_011521067.2:c.1036G>A XP_011519369.1:p.Glu346Lys
XM_011521069.2:c.1036G>A XP_011519371.1:p.Glu346Lys
XM_017020536.2:c.532G>A XP_016876025.1:p.Glu178Lys
XM_017020537.1:c.214G>A XP_016876026.1:p.Glu72Lys
XM_024449336.1:c.1036G>A XP_024305104.1:p.Glu346Lys
NM_052867.4:c.979G>A VV MANE Preferred NP_443099.1:p.Glu327Lys
ENST00000251127.10:c.979G>A ENSP00000251127.6:p.Glu327Lys
ENST00000470333.1:n.1075G>A
ENST00000497170.5:n.1133G>A