Canonical Allele Identifier: CA7035108

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101065553G>A , CM000675.2:g.101065553G>A	GRCh38
NC_000013.10:g.101717905G>A , CM000675.1:g.101717905G>A	GRCh37
NC_000013.9:g.100515906G>A	NCBI36
NG_053176.1:g.356654C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4455C>T MANE Select	ENSP00000251127.6:p.Ile1485=
ENST00000648359.1:c.*75C>T	ENSP00000497465.1:n.*75C>T
ENST00000675150.1:c.4176C>T	ENSP00000502680.1:p.Ile1392=
ENST00000675332.1:c.4542C>T	ENSP00000501955.1:p.Ile1514=
ENST00000676315.1:c.4368C>T	ENSP00000501603.1:p.Ile1456=
ENST00000251127.10:c.4455C>T	ENSP00000251127.6:p.Ile1485=
NM_052867.2:c.4455C>T	NP_443099.1:p.Ile1485=
XM_011521067.1:c.4512C>T	XP_011519369.1:p.Ile1504=
XM_011521068.1:c.4455C>T	XP_011519370.1:p.Ile1485=
XM_011521069.1:c.4425C>T	XP_011519371.1:p.Ile1475=
XM_011521070.1:c.4233C>T	XP_011519372.1:p.Ile1411=
NM_001350748.1:c.4542C>T	NP_001337677.1:p.Ile1514=
NM_001350749.1:c.4455C>T	NP_001337678.1:p.Ile1485=
NM_001350750.1:c.4368C>T	NP_001337679.1:p.Ile1456=
NM_001350751.1:c.4368C>T	NP_001337680.1:p.Ile1456=
NM_052867.3:c.4455C>T	NP_443099.1:p.Ile1485=
XM_011521067.2:c.4512C>T	XP_011519369.1:p.Ile1504=
XM_011521069.2:c.4425C>T	XP_011519371.1:p.Ile1475=
XM_017020536.2:c.4008C>T	XP_016876025.1:p.Ile1336=
XM_017020537.1:c.3690C>T	XP_016876026.1:p.Ile1230=
XM_024449336.1:c.4599C>T	XP_024305104.1:p.Ile1533=
NM_052867.4:c.4455C>T MANE Select	NP_443099.1:p.Ile1485=
NM_001350748.2:c.4542C>T	NP_001337677.1:p.Ile1514=
NM_001350749.2:c.4455C>T	NP_001337678.1:p.Ile1485=
NM_001350750.2:c.4368C>T	NP_001337679.1:p.Ile1456=
NM_001350751.2:c.4368C>T	NP_001337680.1:p.Ile1456=