Canonical Allele Identifier: CA7034956
Gene: NALCN HGNC NCBI
NALCN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101057985G>A , CM000675.2:g.101057985G>A GRCh38
NC_000013.10:g.101710337G>A , CM000675.1:g.101710337G>A GRCh37
NC_000013.9:g.100508338G>A NCBI36
NG_053176.1:g.364222C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.4977C>T (NALCN) MANE Select ENSP00000251127.6:p.Asp1659=
ENST00000648359.1:c.*597C>T (NALCN) ENSP00000497465.1:n.*597C>T
ENST00000675150.1:c.4698C>T (NALCN) ENSP00000502680.1:p.Asp1566=
ENST00000675332.1:c.5064C>T (NALCN) ENSP00000501955.1:p.Asp1688=
ENST00000676315.1:c.4890C>T (NALCN) ENSP00000501603.1:p.Asp1630=
ENST00000251127.10:c.4977C>T (NALCN) ENSP00000251127.6:p.Asp1659=
NM_052867.2:c.4977C>T (NALCN) NP_443099.1:p.Asp1659=
NR_047687.1:n.1545G>A (NALCN-AS1)
XM_011521067.1:c.5034C>T (NALCN) XP_011519369.1:p.Asp1678=
XM_011521068.1:c.4977C>T (NALCN) XP_011519370.1:p.Asp1659=
XM_011521069.1:c.4947C>T (NALCN) XP_011519371.1:p.Asp1649=
XM_011521070.1:c.4755C>T (NALCN) XP_011519372.1:p.Asp1585=
NM_001350748.1:c.5064C>T (NALCN) NP_001337677.1:p.Asp1688=
NM_001350749.1:c.4977C>T (NALCN) NP_001337678.1:p.Asp1659=
NM_001350750.1:c.4890C>T (NALCN) NP_001337679.1:p.Asp1630=
NM_001350751.1:c.4890C>T (NALCN) NP_001337680.1:p.Asp1630=
NM_052867.3:c.4977C>T (NALCN) NP_443099.1:p.Asp1659=
XM_011521067.2:c.5034C>T (NALCN) XP_011519369.1:p.Asp1678=
XM_011521069.2:c.4947C>T (NALCN) XP_011519371.1:p.Asp1649=
XM_017020536.2:c.4530C>T (NALCN) XP_016876025.1:p.Asp1510=
XM_017020537.1:c.4212C>T (NALCN) XP_016876026.1:p.Asp1404=
XM_024449336.1:c.5121C>T (NALCN) XP_024305104.1:p.Asp1707=
NM_052867.4:c.4977C>T (NALCN) MANE Select NP_443099.1:p.Asp1659=
NM_001350748.2:c.5064C>T (NALCN) NP_001337677.1:p.Asp1688=
NM_001350749.2:c.4977C>T (NALCN) NP_001337678.1:p.Asp1659=
NM_001350750.2:c.4890C>T (NALCN) NP_001337679.1:p.Asp1630=
NM_001350751.2:c.4890C>T (NALCN) NP_001337680.1:p.Asp1630=