Canonical Allele Identifier: CA2623581574
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101176286del , CM000675.2:g.101176286del GRCh38
NC_000013.10:g.101828637del , CM000675.1:g.101828637del GRCh37
NC_000013.9:g.100626638del NCBI36
NG_053176.1:g.245925del

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.1839+18del MANE Select ENSP00000251127.6:n.1839+18del
ENST00000467264.2:c.31+18del
ENST00000648359.1:c.1839+18del ENSP00000497465.1:n.1839+18del
ENST00000674840.1:n.1937+18del
ENST00000675150.1:c.1839+18del ENSP00000502680.1:n.1839+18del
ENST00000675332.1:c.1839+18del ENSP00000501955.1:n.1839+18del
ENST00000675802.1:c.1839+18del ENSP00000501818.1:n.1839+18del
ENST00000676315.1:c.1752+18del ENSP00000501603.1:n.1752+18del
ENST00000676439.1:n.2013+18del
ENST00000251127.10:c.1839+18del ENSP00000251127.6:n.1839+18del
ENST00000497170.5:n.1993+18del
NM_052867.2:c.1839+18del NP_443099.1:n.1839+18del
XM_011521067.1:c.1896+18del XP_011519369.1:n.1896+18del
XM_011521068.1:c.1839+18del XP_011519370.1:n.1839+18del
XM_011521069.1:c.1809+18del XP_011519371.1:n.1809+18del
XM_011521070.1:c.1896+18del XP_011519372.1:n.1896+18del
NM_001350748.1:c.1839+18del NP_001337677.1:n.1839+18del
NM_001350749.1:c.1839+18del NP_001337678.1:n.1839+18del
NM_001350750.1:c.1752+18del NP_001337679.1:n.1752+18del
NM_001350751.1:c.1752+18del NP_001337680.1:n.1752+18del
NM_052867.3:c.1839+18del NP_443099.1:n.1839+18del
XM_011521067.2:c.1896+18del XP_011519369.1:n.1896+18del
XM_011521069.2:c.1809+18del XP_011519371.1:n.1809+18del
XM_017020536.2:c.1392+18del XP_016876025.1:n.1392+18del
XM_017020537.1:c.1074+18del XP_016876026.1:n.1074+18del
XM_024449336.1:c.1896+18del XP_024305104.1:n.1896+18del
NM_052867.4:c.1839+18del MANE Select NP_443099.1:n.1839+18del
NM_001350748.2:c.1839+18del NP_001337677.1:n.1839+18del
NM_001350749.2:c.1839+18del NP_001337678.1:n.1839+18del
NM_001350750.2:c.1752+18del NP_001337679.1:n.1752+18del
NM_001350751.2:c.1752+18del NP_001337680.1:n.1752+18del