Canonical Allele Identifier: CA484552387

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733983G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081632G>A , CM000675.2:g.101081632G>A	GRCh38
NC_000013.10:g.101733983G>A , CM000675.1:g.101733983G>A	GRCh37
NC_000013.9:g.100531984G>A	NCBI36
NG_053176.1:g.340575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3780C>T MANE Select	ENSP00000251127.6:p.Ile1260=
ENST00000648359.1:c.3780C>T	ENSP00000497465.1:p.Ile1260=
ENST00000675150.1:c.3501C>T	ENSP00000502680.1:p.Ile1167=
ENST00000675332.1:c.3867C>T	ENSP00000501955.1:p.Ile1289=
ENST00000676315.1:c.3693C>T	ENSP00000501603.1:p.Ile1231=
ENST00000251127.10:c.3780C>T	ENSP00000251127.6:p.Ile1260=
NM_052867.2:c.3780C>T	NP_443099.1:p.Ile1260=
XM_011521067.1:c.3837C>T	XP_011519369.1:p.Ile1279=
XM_011521068.1:c.3780C>T	XP_011519370.1:p.Ile1260=
XM_011521069.1:c.3750C>T	XP_011519371.1:p.Ile1250=
XM_011521070.1:c.3558C>T	XP_011519372.1:p.Ile1186=
NM_001350748.1:c.3867C>T	NP_001337677.1:p.Ile1289=
NM_001350749.1:c.3780C>T	NP_001337678.1:p.Ile1260=
NM_001350750.1:c.3693C>T	NP_001337679.1:p.Ile1231=
NM_001350751.1:c.3693C>T	NP_001337680.1:p.Ile1231=
NM_052867.3:c.3780C>T	NP_443099.1:p.Ile1260=
XM_011521067.2:c.3837C>T	XP_011519369.1:p.Ile1279=
XM_011521069.2:c.3750C>T	XP_011519371.1:p.Ile1250=
XM_017020536.2:c.3333C>T	XP_016876025.1:p.Ile1111=
XM_017020537.1:c.3015C>T	XP_016876026.1:p.Ile1005=
XM_024449336.1:c.3924C>T	XP_024305104.1:p.Ile1308=
NM_052867.4:c.3780C>T MANE Select	NP_443099.1:p.Ile1260=
NM_001350748.2:c.3867C>T	NP_001337677.1:p.Ile1289=
NM_001350749.2:c.3780C>T	NP_001337678.1:p.Ile1260=
NM_001350750.2:c.3693C>T	NP_001337679.1:p.Ile1231=
NM_001350751.2:c.3693C>T	NP_001337680.1:p.Ile1231=