Canonical Allele Identifier: CA7035127

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101067948T>G , CM000675.2:g.101067948T>G	GRCh38
NC_000013.10:g.101720300T>G , CM000675.1:g.101720300T>G	GRCh37
NC_000013.9:g.100518301T>G	NCBI36
NG_053176.1:g.354259A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4416A>C MANE Select	ENSP00000251127.6:p.Ile1472=
ENST00000648359.1:c.4416A>C	ENSP00000497465.1:p.Ile1472=
ENST00000675150.1:c.4137A>C	ENSP00000502680.1:p.Ile1379=
ENST00000675332.1:c.4503A>C	ENSP00000501955.1:p.Ile1501=
ENST00000676315.1:c.4329A>C	ENSP00000501603.1:p.Ile1443=
ENST00000251127.10:c.4416A>C	ENSP00000251127.6:p.Ile1472=
NM_052867.2:c.4416A>C	NP_443099.1:p.Ile1472=
XM_011521067.1:c.4473A>C	XP_011519369.1:p.Ile1491=
XM_011521068.1:c.4416A>C	XP_011519370.1:p.Ile1472=
XM_011521069.1:c.4386A>C	XP_011519371.1:p.Ile1462=
XM_011521070.1:c.4194A>C	XP_011519372.1:p.Ile1398=
NM_001350748.1:c.4503A>C	NP_001337677.1:p.Ile1501=
NM_001350749.1:c.4416A>C	NP_001337678.1:p.Ile1472=
NM_001350750.1:c.4329A>C	NP_001337679.1:p.Ile1443=
NM_001350751.1:c.4329A>C	NP_001337680.1:p.Ile1443=
NM_052867.3:c.4416A>C	NP_443099.1:p.Ile1472=
XM_011521067.2:c.4473A>C	XP_011519369.1:p.Ile1491=
XM_011521069.2:c.4386A>C	XP_011519371.1:p.Ile1462=
XM_017020536.2:c.3969A>C	XP_016876025.1:p.Ile1323=
XM_017020537.1:c.3651A>C	XP_016876026.1:p.Ile1217=
XM_024449336.1:c.4560A>C	XP_024305104.1:p.Ile1520=
NM_052867.4:c.4416A>C MANE Select	NP_443099.1:p.Ile1472=
NM_001350748.2:c.4503A>C	NP_001337677.1:p.Ile1501=
NM_001350749.2:c.4416A>C	NP_001337678.1:p.Ile1472=
NM_001350750.2:c.4329A>C	NP_001337679.1:p.Ile1443=
NM_001350751.2:c.4329A>C	NP_001337680.1:p.Ile1443=