Canonical Allele Identifier: CA2114432055
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101176384_101176386delinsGGT , CM000675.2:g.101176384_101176386delinsGGT GRCh38
NC_000013.10:g.101828735_101828737delinsGGT , CM000675.1:g.101828735_101828737delinsGGT GRCh37
NC_000013.9:g.100626736_100626738delinsGGT NCBI36
NG_053176.1:g.245821_245823delinsACC

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.1765-12_1765-10delinsACC MANE Select ENSP00000251127.6:n.1765-12_1765-10delins...
ENST00000648359.1:c.1765-12_1765-10delinsACC ENSP00000497465.1:n.1765-12_1765-10delins...
ENST00000674840.1:n.1863-12_1863-10delinsACC
ENST00000675150.1:c.1765-12_1765-10delinsACC ENSP00000502680.1:n.1765-12_1765-10delins...
ENST00000675332.1:c.1765-12_1765-10delinsACC ENSP00000501955.1:n.1765-12_1765-10delins...
ENST00000675802.1:c.1765-12_1765-10delinsACC ENSP00000501818.1:n.1765-12_1765-10delins...
ENST00000675891.1:n.605-12_605-10delinsACC
ENST00000676315.1:c.1678-12_1678-10delinsACC ENSP00000501603.1:n.1678-12_1678-10delins...
ENST00000676439.1:n.1939-12_1939-10delinsACC
ENST00000251127.10:c.1765-12_1765-10delinsACC ENSP00000251127.6:n.1765-12_1765-10delins...
ENST00000497170.5:n.1919-12_1919-10delinsACC
NM_052867.2:c.1765-12_1765-10delinsACC NP_443099.1:n.1765-12_1765-10delinsACC
XM_011521067.1:c.1822-12_1822-10delinsACC XP_011519369.1:n.1822-12_1822-10delinsACC...
XM_011521068.1:c.1765-12_1765-10delinsACC XP_011519370.1:n.1765-12_1765-10delinsACC...
XM_011521069.1:c.1735-12_1735-10delinsACC XP_011519371.1:n.1735-12_1735-10delinsACC...
XM_011521070.1:c.1822-12_1822-10delinsACC XP_011519372.1:n.1822-12_1822-10delinsACC...
NM_001350748.1:c.1765-12_1765-10delinsACC NP_001337677.1:n.1765-12_1765-10delinsACC...
NM_001350749.1:c.1765-12_1765-10delinsACC NP_001337678.1:n.1765-12_1765-10delinsACC...
NM_001350750.1:c.1678-12_1678-10delinsACC NP_001337679.1:n.1678-12_1678-10delinsACC...
NM_001350751.1:c.1678-12_1678-10delinsACC NP_001337680.1:n.1678-12_1678-10delinsACC...
NM_052867.3:c.1765-12_1765-10delinsACC NP_443099.1:n.1765-12_1765-10delinsACC
XM_011521067.2:c.1822-12_1822-10delinsACC XP_011519369.1:n.1822-12_1822-10delinsACC...
XM_011521069.2:c.1735-12_1735-10delinsACC XP_011519371.1:n.1735-12_1735-10delinsACC...
XM_017020536.2:c.1318-12_1318-10delinsACC XP_016876025.1:n.1318-12_1318-10delinsACC...
XM_017020537.1:c.1000-12_1000-10delinsACC XP_016876026.1:n.1000-12_1000-10delinsACC...
XM_024449336.1:c.1822-12_1822-10delinsACC XP_024305104.1:n.1822-12_1822-10delinsACC...
NM_052867.4:c.1765-12_1765-10delinsACC MANE Select NP_443099.1:n.1765-12_1765-10delinsACC
NM_001350748.2:c.1765-12_1765-10delinsACC NP_001337677.1:n.1765-12_1765-10delinsACC...
NM_001350749.2:c.1765-12_1765-10delinsACC NP_001337678.1:n.1765-12_1765-10delinsACC...
NM_001350750.2:c.1678-12_1678-10delinsACC NP_001337679.1:n.1678-12_1678-10delinsACC...
NM_001350751.2:c.1678-12_1678-10delinsACC NP_001337680.1:n.1678-12_1678-10delinsACC...