Canonical Allele Identifier: CA388704794
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101292066G>T , CM000675.2:g.101292066G>T GRCh38
NC_000013.10:g.101944417G>T , CM000675.1:g.101944417G>T GRCh37
NC_000013.9:g.100742418G>T NCBI36
NG_053176.1:g.130141C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.971C>A MANE Select ENSP00000251127.6:p.Thr324Lys
ENST00000648359.1:c.971C>A ENSP00000497465.1:p.Thr324Lys
ENST00000674840.1:n.1069C>A
ENST00000674904.1:n.1051C>A
ENST00000675150.1:c.971C>A ENSP00000502680.1:p.Thr324Lys
ENST00000675332.1:c.971C>A ENSP00000501955.1:p.Thr324Lys
ENST00000675415.1:n.1154C>A
ENST00000675594.1:c.*408C>A ENSP00000502490.1:n.*408C>A
ENST00000675802.1:c.971C>A ENSP00000501818.1:p.Thr324Lys
ENST00000676315.1:c.971C>A ENSP00000501603.1:p.Thr324Lys
ENST00000676439.1:n.1145C>A
ENST00000251127.10:c.971C>A ENSP00000251127.6:p.Thr324Lys
ENST00000470333.1:n.1067C>A
ENST00000497170.5:n.1125C>A
NM_052867.2:c.971C>A NP_443099.1:p.Thr324Lys
XM_011521067.1:c.1028C>A XP_011519369.1:p.Thr343Lys
XM_011521068.1:c.971C>A XP_011519370.1:p.Thr324Lys
XM_011521069.1:c.1028C>A XP_011519371.1:p.Thr343Lys
XM_011521070.1:c.1028C>A XP_011519372.1:p.Thr343Lys
NM_001350748.1:c.971C>A NP_001337677.1:p.Thr324Lys
NM_001350749.1:c.971C>A NP_001337678.1:p.Thr324Lys
NM_001350750.1:c.971C>A NP_001337679.1:p.Thr324Lys
NM_001350751.1:c.971C>A NP_001337680.1:p.Thr324Lys
NM_052867.3:c.971C>A NP_443099.1:p.Thr324Lys
XM_011521067.2:c.1028C>A XP_011519369.1:p.Thr343Lys
XM_011521069.2:c.1028C>A XP_011519371.1:p.Thr343Lys
XM_017020536.2:c.524C>A XP_016876025.1:p.Thr175Lys
XM_017020537.1:c.206C>A XP_016876026.1:p.Thr69Lys
XM_024449336.1:c.1028C>A XP_024305104.1:p.Thr343Lys
NM_052867.4:c.971C>A MANE Select NP_443099.1:p.Thr324Lys
NM_001350748.2:c.971C>A NP_001337677.1:p.Thr324Lys
NM_001350749.2:c.971C>A NP_001337678.1:p.Thr324Lys
NM_001350750.2:c.971C>A NP_001337679.1:p.Thr324Lys
NM_001350751.2:c.971C>A NP_001337680.1:p.Thr324Lys