Canonical Allele Identifier: CA10581444
Gene: NALCN HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 235833
ClinVar RCV Id: RCV000224757
dbSNP Id: rs878853130

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101103212A>G , CM000675.2:g.101103212A>G GRCh38
NC_000013.10:g.101755563A>G , CM000675.1:g.101755563A>G GRCh37
NC_000013.9:g.100553564A>G NCBI36
NG_053176.1:g.318995T>C

Transcript Alleles

HGVS Amino-acid change
NM_052867.2:c.3017T>C VV NP_443099.1:p.Val1006Ala
XM_011521067.1:c.3074T>C XP_011519369.1:p.Val1025Ala
XM_011521068.1:c.3017T>C XP_011519370.1:p.Val1006Ala
XM_011521069.1:c.2987T>C XP_011519371.1:p.Val996Ala
XM_011521070.1:c.2795T>C XP_011519372.1:p.Val932Ala
NM_001350748.1:c.3104T>C VV NP_001337677.1:p.Val1035Ala
NM_001350749.1:c.3017T>C VV NP_001337678.1:p.Val1006Ala
NM_001350750.1:c.2930T>C VV NP_001337679.1:p.Val977Ala
NM_001350751.1:c.2930T>C VV NP_001337680.1:p.Val977Ala
NM_052867.3:c.3017T>C VV NP_443099.1:p.Val1006Ala
XM_011521067.2:c.3074T>C XP_011519369.1:p.Val1025Ala
XM_011521069.2:c.2987T>C XP_011519371.1:p.Val996Ala
XM_017020536.2:c.2570T>C XP_016876025.1:p.Val857Ala
XM_017020537.1:c.2252T>C XP_016876026.1:p.Val751Ala
XM_024449336.1:c.3161T>C XP_024305104.1:p.Val1054Ala
NM_052867.4:c.3017T>C VV MANE Preferred NP_443099.1:p.Val1006Ala
ENST00000251127.10:c.3017T>C ENSP00000251127.6:p.Val1006Ala