Canonical Allele Identifier: CA388705271
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101376713C>T , CM000675.2:g.101376713C>T GRCh38
NC_000013.10:g.102029064C>T , CM000675.1:g.102029064C>T GRCh37
NC_000013.9:g.100827065C>T NCBI36
NG_053176.1:g.45494G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.631G>A MANE Select ENSP00000251127.6:p.Asp211Asn
ENST00000376200.6:c.631G>A ENSP00000365373.5:p.Asp211Asn
ENST00000648359.1:c.631G>A ENSP00000497465.1:p.Asp211Asn
ENST00000674840.1:n.729G>A
ENST00000674904.1:n.711G>A
ENST00000675150.1:c.631G>A ENSP00000502680.1:p.Asp211Asn
ENST00000675332.1:c.631G>A ENSP00000501955.1:p.Asp211Asn
ENST00000675415.1:n.814G>A
ENST00000675594.1:c.631G>A ENSP00000502490.1:p.Asp211Asn
ENST00000675802.1:c.631G>A ENSP00000501818.1:p.Asp211Asn
ENST00000676315.1:c.631G>A ENSP00000501603.1:p.Asp211Asn
ENST00000676357.1:n.851G>A
ENST00000676439.1:n.805G>A
ENST00000251127.10:c.631G>A ENSP00000251127.6:p.Asp211Asn
ENST00000376200.5:c.631G>A ENSP00000365373.5:p.Asp211Asn
ENST00000470333.1:n.727G>A
ENST00000497170.5:n.820G>A
NM_052867.2:c.631G>A NP_443099.1:p.Asp211Asn
XM_011521067.1:c.688G>A XP_011519369.1:p.Asp230Asn
XM_011521068.1:c.631G>A XP_011519370.1:p.Asp211Asn
XM_011521069.1:c.688G>A XP_011519371.1:p.Asp230Asn
XM_011521070.1:c.688G>A XP_011519372.1:p.Asp230Asn
NM_001350748.1:c.631G>A NP_001337677.1:p.Asp211Asn
NM_001350749.1:c.631G>A NP_001337678.1:p.Asp211Asn
NM_001350750.1:c.631G>A NP_001337679.1:p.Asp211Asn
NM_001350751.1:c.631G>A NP_001337680.1:p.Asp211Asn
NM_052867.3:c.631G>A NP_443099.1:p.Asp211Asn
XM_011521067.2:c.688G>A XP_011519369.1:p.Asp230Asn
XM_011521069.2:c.688G>A XP_011519371.1:p.Asp230Asn
XM_024449336.1:c.688G>A XP_024305104.1:p.Asp230Asn
NM_052867.4:c.631G>A MANE Select NP_443099.1:p.Asp211Asn
NM_001350748.2:c.631G>A NP_001337677.1:p.Asp211Asn
NM_001350749.2:c.631G>A NP_001337678.1:p.Asp211Asn
NM_001350750.2:c.631G>A NP_001337679.1:p.Asp211Asn
NM_001350751.2:c.631G>A NP_001337680.1:p.Asp211Asn