Canonical Allele Identifier: CA2114398043
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101103216T= , CM000675.2:g.101103216T= GRCh38
NC_000013.10:g.101755567T= , CM000675.1:g.101755567T= GRCh37
NC_000013.9:g.100553568T= NCBI36
NG_053176.1:g.318991A=

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.3013A= MANE Select ENSP00000251127.6:p.Lys1005=
ENST00000648359.1:c.3013A= ENSP00000497465.1:p.Lys1005=
ENST00000675150.1:c.2734A= ENSP00000502680.1:p.Lys912=
ENST00000675332.1:c.3100A= ENSP00000501955.1:p.Lys1034=
ENST00000676315.1:c.2926A= ENSP00000501603.1:p.Lys976=
ENST00000251127.10:c.3013A= ENSP00000251127.6:p.Lys1005=
NM_052867.2:c.3013A= NP_443099.1:p.Lys1005=
XM_011521067.1:c.3070A= XP_011519369.1:p.Lys1024=
XM_011521068.1:c.3013A= XP_011519370.1:p.Lys1005=
XM_011521069.1:c.2983A= XP_011519371.1:p.Lys995=
XM_011521070.1:c.2791A= XP_011519372.1:p.Lys931=
NM_001350748.1:c.3100A= NP_001337677.1:p.Lys1034=
NM_001350749.1:c.3013A= NP_001337678.1:p.Lys1005=
NM_001350750.1:c.2926A= NP_001337679.1:p.Lys976=
NM_001350751.1:c.2926A= NP_001337680.1:p.Lys976=
NM_052867.3:c.3013A= NP_443099.1:p.Lys1005=
XM_011521067.2:c.3070A= XP_011519369.1:p.Lys1024=
XM_011521069.2:c.2983A= XP_011519371.1:p.Lys995=
XM_017020536.2:c.2566A= XP_016876025.1:p.Lys856=
XM_017020537.1:c.2248A= XP_016876026.1:p.Lys750=
XM_024449336.1:c.3157A= XP_024305104.1:p.Lys1053=
NM_052867.4:c.3013A= MANE Select NP_443099.1:p.Lys1005=
NM_001350748.2:c.3100A= NP_001337677.1:p.Lys1034=
NM_001350749.2:c.3013A= NP_001337678.1:p.Lys1005=
NM_001350750.2:c.2926A= NP_001337679.1:p.Lys976=
NM_001350751.2:c.2926A= NP_001337680.1:p.Lys976=