Canonical Allele Identifier: CA2114388953
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101081852_101081856delinsACTAT , CM000675.2:g.101081852_101081856delinsACTAT GRCh38
NC_000013.10:g.101734203_101734207delinsACTAT , CM000675.1:g.101734203_101734207delinsACTAT GRCh37
NC_000013.9:g.100532204_100532208delinsACTAT NCBI36
NG_053176.1:g.340351_340355delinsATAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.3766-210_3766-206delinsATAGT MANE Select ENSP00000251127.6:n.3766-210_3766-206delinsATAGT
ENST00000648359.1:c.3766-210_3766-206delinsATAGT ENSP00000497465.1:n.3766-210_3766-206delinsATAGT
ENST00000675150.1:c.3487-210_3487-206delinsATAGT ENSP00000502680.1:n.3487-210_3487-206delinsATAGT
ENST00000675332.1:c.3853-210_3853-206delinsATAGT ENSP00000501955.1:n.3853-210_3853-206delinsATAGT
ENST00000676315.1:c.3679-210_3679-206delinsATAGT ENSP00000501603.1:n.3679-210_3679-206delinsATAGT
ENST00000251127.10:c.3766-210_3766-206delinsATAGT ENSP00000251127.6:n.3766-210_3766-206delinsATAGT
NM_052867.2:c.3766-210_3766-206delinsATAGT NP_443099.1:n.3766-210_3766-206delinsATAGT
XM_011521067.1:c.3823-210_3823-206delinsATAGT XP_011519369.1:n.3823-210_3823-206delinsATAGT
XM_011521068.1:c.3766-210_3766-206delinsATAGT XP_011519370.1:n.3766-210_3766-206delinsATAGT
XM_011521069.1:c.3736-210_3736-206delinsATAGT XP_011519371.1:n.3736-210_3736-206delinsATAGT
XM_011521070.1:c.3544-210_3544-206delinsATAGT XP_011519372.1:n.3544-210_3544-206delinsATAGT
NM_001350748.1:c.3853-210_3853-206delinsATAGT NP_001337677.1:n.3853-210_3853-206delinsATAGT
NM_001350749.1:c.3766-210_3766-206delinsATAGT NP_001337678.1:n.3766-210_3766-206delinsATAGT
NM_001350750.1:c.3679-210_3679-206delinsATAGT NP_001337679.1:n.3679-210_3679-206delinsATAGT
NM_001350751.1:c.3679-210_3679-206delinsATAGT NP_001337680.1:n.3679-210_3679-206delinsATAGT
NM_052867.3:c.3766-210_3766-206delinsATAGT NP_443099.1:n.3766-210_3766-206delinsATAGT
XM_011521067.2:c.3823-210_3823-206delinsATAGT XP_011519369.1:n.3823-210_3823-206delinsATAGT
XM_011521069.2:c.3736-210_3736-206delinsATAGT XP_011519371.1:n.3736-210_3736-206delinsATAGT
XM_017020536.2:c.3319-210_3319-206delinsATAGT XP_016876025.1:n.3319-210_3319-206delinsATAGT
XM_017020537.1:c.3001-210_3001-206delinsATAGT XP_016876026.1:n.3001-210_3001-206delinsATAGT
XM_024449336.1:c.3910-210_3910-206delinsATAGT XP_024305104.1:n.3910-210_3910-206delinsATAGT
NM_052867.4:c.3766-210_3766-206delinsATAGT MANE Select NP_443099.1:n.3766-210_3766-206delinsATAGT
NM_001350748.2:c.3853-210_3853-206delinsATAGT NP_001337677.1:n.3853-210_3853-206delinsATAGT
NM_001350749.2:c.3766-210_3766-206delinsATAGT NP_001337678.1:n.3766-210_3766-206delinsATAGT
NM_001350750.2:c.3679-210_3679-206delinsATAGT NP_001337679.1:n.3679-210_3679-206delinsATAGT
NM_001350751.2:c.3679-210_3679-206delinsATAGT NP_001337680.1:n.3679-210_3679-206delinsATAGT