Canonical Allele Identifier: CA2114388865
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101081630A= , CM000675.2:g.101081630A= GRCh38
NC_000013.10:g.101733981A= , CM000675.1:g.101733981A= GRCh37
NC_000013.9:g.100531982A= NCBI36
NG_053176.1:g.340577T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.3782T= MANE Select ENSP00000251127.6:p.Ile1261=
ENST00000648359.1:c.3782T= ENSP00000497465.1:p.Ile1261=
ENST00000675150.1:c.3503T= ENSP00000502680.1:p.Ile1168=
ENST00000675332.1:c.3869T= ENSP00000501955.1:p.Ile1290=
ENST00000676315.1:c.3695T= ENSP00000501603.1:p.Ile1232=
ENST00000251127.10:c.3782T= ENSP00000251127.6:p.Ile1261=
NM_052867.2:c.3782T= NP_443099.1:p.Ile1261=
XM_011521067.1:c.3839T= XP_011519369.1:p.Ile1280=
XM_011521068.1:c.3782T= XP_011519370.1:p.Ile1261=
XM_011521069.1:c.3752T= XP_011519371.1:p.Ile1251=
XM_011521070.1:c.3560T= XP_011519372.1:p.Ile1187=
NM_001350748.1:c.3869T= NP_001337677.1:p.Ile1290=
NM_001350749.1:c.3782T= NP_001337678.1:p.Ile1261=
NM_001350750.1:c.3695T= NP_001337679.1:p.Ile1232=
NM_001350751.1:c.3695T= NP_001337680.1:p.Ile1232=
NM_052867.3:c.3782T= NP_443099.1:p.Ile1261=
XM_011521067.2:c.3839T= XP_011519369.1:p.Ile1280=
XM_011521069.2:c.3752T= XP_011519371.1:p.Ile1251=
XM_017020536.2:c.3335T= XP_016876025.1:p.Ile1112=
XM_017020537.1:c.3017T= XP_016876026.1:p.Ile1006=
XM_024449336.1:c.3926T= XP_024305104.1:p.Ile1309=
NM_052867.4:c.3782T= MANE Select NP_443099.1:p.Ile1261=
NM_001350748.2:c.3869T= NP_001337677.1:p.Ile1290=
NM_001350749.2:c.3782T= NP_001337678.1:p.Ile1261=
NM_001350750.2:c.3695T= NP_001337679.1:p.Ile1232=
NM_001350751.2:c.3695T= NP_001337680.1:p.Ile1232=