Canonical Allele Identifier: CA7035453
Gene: NALCN HGNC NCBI

Linked Data

dbSNP Id: rs748898736

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101095560del , CM000675.2:g.101095560del GRCh38
NC_000013.10:g.101747911del , CM000675.1:g.101747911del GRCh37
NC_000013.9:g.100545912del NCBI36
NG_053176.1:g.326653del

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.3269+20del MANE Select ENSP00000251127.6:n.3269+20del
ENST00000648359.1:c.3269+20del ENSP00000497465.1:n.3269+20del
ENST00000675150.1:c.2990+20del ENSP00000502680.1:n.2990+20del
ENST00000675332.1:c.3356+20del ENSP00000501955.1:n.3356+20del
ENST00000676315.1:c.3182+20del ENSP00000501603.1:n.3182+20del
ENST00000251127.10:c.3269+20del ENSP00000251127.6:n.3269+20del
NM_052867.2:c.3269+20del NP_443099.1:n.3269+20del
XM_011521067.1:c.3326+20del XP_011519369.1:n.3326+20del
XM_011521068.1:c.3269+20del XP_011519370.1:n.3269+20del
XM_011521069.1:c.3239+20del XP_011519371.1:n.3239+20del
XM_011521070.1:c.3047+20del XP_011519372.1:n.3047+20del
NM_001350748.1:c.3356+20del NP_001337677.1:n.3356+20del
NM_001350749.1:c.3269+20del NP_001337678.1:n.3269+20del
NM_001350750.1:c.3182+20del NP_001337679.1:n.3182+20del
NM_001350751.1:c.3182+20del NP_001337680.1:n.3182+20del
NM_052867.3:c.3269+20del NP_443099.1:n.3269+20del
XM_011521067.2:c.3326+20del XP_011519369.1:n.3326+20del
XM_011521069.2:c.3239+20del XP_011519371.1:n.3239+20del
XM_017020536.2:c.2822+20del XP_016876025.1:n.2822+20del
XM_017020537.1:c.2504+20del XP_016876026.1:n.2504+20del
XM_024449336.1:c.3413+20del XP_024305104.1:n.3413+20del
NM_052867.4:c.3269+20del MANE Select NP_443099.1:n.3269+20del
NM_001350748.2:c.3356+20del NP_001337677.1:n.3356+20del
NM_001350749.2:c.3269+20del NP_001337678.1:n.3269+20del
NM_001350750.2:c.3182+20del NP_001337679.1:n.3182+20del
NM_001350751.2:c.3182+20del NP_001337680.1:n.3182+20del