Canonical Allele Identifier: CA2800371245

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101176390_101176391insGTTTAACTTTTATCTAATAT , CM000675.2:g.101176390_101176391insGTTTAACTTTTATCTAATAT	GRCh38
NC_000013.10:g.101828741_101828742insGTTTAACTTTTATCTAATAT , CM000675.1:g.101828741_101828742insGTTTAACTTTTATCTAATAT	GRCh37
NC_000013.9:g.100626742_100626743insGTTTAACTTTTATCTAATAT	NCBI36
NG_053176.1:g.245816_245817insATATTAGATAAAAGTTAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC MANE Select	ENSP00000251127.6:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000648359.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	ENSP00000497465.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000674840.1:n.1863-17_1863-16insATATTAGATAAAAGTTAAAC
ENST00000675150.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	ENSP00000502680.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000675332.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	ENSP00000501955.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000675802.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	ENSP00000501818.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000675891.1:n.605-17_605-16insATATTAGATAAAAGTTAAAC
ENST00000676315.1:c.1678-17_1678-16insATATTAGATAAAAGTTAAAC	ENSP00000501603.1:n.1678-17_1678-16insATATTAGATAAAAGTTAAAC
ENST00000676439.1:n.1939-17_1939-16insATATTAGATAAAAGTTAAAC
ENST00000251127.10:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	ENSP00000251127.6:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
ENST00000497170.5:n.1919-17_1919-16insATATTAGATAAAAGTTAAAC
NM_052867.2:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_443099.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
XM_011521067.1:c.1822-17_1822-16insATATTAGATAAAAGTTAAAC	XP_011519369.1:n.1822-17_1822-16insATATTAGATAAAAGTTAAAC
XM_011521068.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	XP_011519370.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
XM_011521069.1:c.1735-17_1735-16insATATTAGATAAAAGTTAAAC	XP_011519371.1:n.1735-17_1735-16insATATTAGATAAAAGTTAAAC
XM_011521070.1:c.1822-17_1822-16insATATTAGATAAAAGTTAAAC	XP_011519372.1:n.1822-17_1822-16insATATTAGATAAAAGTTAAAC
NM_001350748.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_001337677.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
NM_001350749.1:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_001337678.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
NM_001350750.1:c.1678-17_1678-16insATATTAGATAAAAGTTAAAC	NP_001337679.1:n.1678-17_1678-16insATATTAGATAAAAGTTAAAC
NM_001350751.1:c.1678-17_1678-16insATATTAGATAAAAGTTAAAC	NP_001337680.1:n.1678-17_1678-16insATATTAGATAAAAGTTAAAC
NM_052867.3:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_443099.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
XM_011521067.2:c.1822-17_1822-16insATATTAGATAAAAGTTAAAC	XP_011519369.1:n.1822-17_1822-16insATATTAGATAAAAGTTAAAC
XM_011521069.2:c.1735-17_1735-16insATATTAGATAAAAGTTAAAC	XP_011519371.1:n.1735-17_1735-16insATATTAGATAAAAGTTAAAC
XM_017020536.2:c.1318-17_1318-16insATATTAGATAAAAGTTAAAC	XP_016876025.1:n.1318-17_1318-16insATATTAGATAAAAGTTAAAC
XM_017020537.1:c.1000-17_1000-16insATATTAGATAAAAGTTAAAC	XP_016876026.1:n.1000-17_1000-16insATATTAGATAAAAGTTAAAC
XM_024449336.1:c.1822-17_1822-16insATATTAGATAAAAGTTAAAC	XP_024305104.1:n.1822-17_1822-16insATATTAGATAAAAGTTAAAC
NM_052867.4:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC MANE Select	NP_443099.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
NM_001350748.2:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_001337677.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
NM_001350749.2:c.1765-17_1765-16insATATTAGATAAAAGTTAAAC	NP_001337678.1:n.1765-17_1765-16insATATTAGATAAAAGTTAAAC
NM_001350750.2:c.1678-17_1678-16insATATTAGATAAAAGTTAAAC	NP_001337679.1:n.1678-17_1678-16insATATTAGATAAAAGTTAAAC
NM_001350751.2:c.1678-17_1678-16insATATTAGATAAAAGTTAAAC	NP_001337680.1:n.1678-17_1678-16insATATTAGATAAAAGTTAAAC