Canonical Allele Identifier: CA388705533
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101376828C>A , CM000675.2:g.101376828C>A GRCh38
NC_000013.10:g.102029179C>A , CM000675.1:g.102029179C>A GRCh37
NC_000013.9:g.100827180C>A NCBI36
NG_053176.1:g.45379G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.516G>T MANE Select ENSP00000251127.6:p.Lys172Asn
ENST00000376200.6:c.516G>T ENSP00000365373.5:p.Lys172Asn
ENST00000648359.1:c.516G>T ENSP00000497465.1:p.Lys172Asn
ENST00000674840.1:n.614G>T
ENST00000674904.1:n.596G>T
ENST00000675150.1:c.516G>T ENSP00000502680.1:p.Lys172Asn
ENST00000675332.1:c.516G>T ENSP00000501955.1:p.Lys172Asn
ENST00000675415.1:n.699G>T
ENST00000675594.1:c.516G>T ENSP00000502490.1:p.Lys172Asn
ENST00000675802.1:c.516G>T ENSP00000501818.1:p.Lys172Asn
ENST00000676315.1:c.516G>T ENSP00000501603.1:p.Lys172Asn
ENST00000676357.1:n.736G>T
ENST00000676439.1:n.690G>T
ENST00000251127.10:c.516G>T ENSP00000251127.6:p.Lys172Asn
ENST00000376200.5:c.516G>T ENSP00000365373.5:p.Lys172Asn
ENST00000470333.1:n.612G>T
ENST00000497170.5:n.705G>T
NM_052867.2:c.516G>T NP_443099.1:p.Lys172Asn
XM_011521067.1:c.573G>T XP_011519369.1:p.Lys191Asn
XM_011521068.1:c.516G>T XP_011519370.1:p.Lys172Asn
XM_011521069.1:c.573G>T XP_011519371.1:p.Lys191Asn
XM_011521070.1:c.573G>T XP_011519372.1:p.Lys191Asn
NM_001350748.1:c.516G>T NP_001337677.1:p.Lys172Asn
NM_001350749.1:c.516G>T NP_001337678.1:p.Lys172Asn
NM_001350750.1:c.516G>T NP_001337679.1:p.Lys172Asn
NM_001350751.1:c.516G>T NP_001337680.1:p.Lys172Asn
NM_052867.3:c.516G>T NP_443099.1:p.Lys172Asn
XM_011521067.2:c.573G>T XP_011519369.1:p.Lys191Asn
XM_011521069.2:c.573G>T XP_011519371.1:p.Lys191Asn
XM_024449336.1:c.573G>T XP_024305104.1:p.Lys191Asn
NM_052867.4:c.516G>T MANE Select NP_443099.1:p.Lys172Asn
NM_001350748.2:c.516G>T NP_001337677.1:p.Lys172Asn
NM_001350749.2:c.516G>T NP_001337678.1:p.Lys172Asn
NM_001350750.2:c.516G>T NP_001337679.1:p.Lys172Asn
NM_001350751.2:c.516G>T NP_001337680.1:p.Lys172Asn