Canonical Allele Identifier: CA484554703

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101795455C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101143104C>T , CM000675.2:g.101143104C>T	GRCh38
NC_000013.10:g.101795455C>T , CM000675.1:g.101795455C>T	GRCh37
NC_000013.9:g.100593456C>T	NCBI36
NG_053176.1:g.279103G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.2094G>A MANE Select	ENSP00000251127.6:p.Glu698=
ENST00000467264.2:c.286G>A
ENST00000648359.1:c.2094G>A	ENSP00000497465.1:p.Glu698=
ENST00000675150.1:c.1840-18423G>A	ENSP00000502680.1:n.1840-18423G>A
ENST00000675332.1:c.2094G>A	ENSP00000501955.1:p.Glu698=
ENST00000675802.1:c.2094G>A	ENSP00000501818.1:p.Glu698=
ENST00000676315.1:c.2007G>A	ENSP00000501603.1:p.Glu669=
ENST00000251127.10:c.2094G>A	ENSP00000251127.6:p.Glu698=
ENST00000467264.1:n.118G>A
ENST00000497170.5:n.2248G>A
NM_052867.2:c.2094G>A	NP_443099.1:p.Glu698=
XM_011521067.1:c.2151G>A	XP_011519369.1:p.Glu717=
XM_011521068.1:c.2094G>A	XP_011519370.1:p.Glu698=
XM_011521069.1:c.2064G>A	XP_011519371.1:p.Glu688=
XM_011521070.1:c.1897-18423G>A	XP_011519372.1:n.1897-18423G>A
NM_001350748.1:c.2094G>A	NP_001337677.1:p.Glu698=
NM_001350749.1:c.2094G>A	NP_001337678.1:p.Glu698=
NM_001350750.1:c.2007G>A	NP_001337679.1:p.Glu669=
NM_001350751.1:c.2007G>A	NP_001337680.1:p.Glu669=
NM_052867.3:c.2094G>A	NP_443099.1:p.Glu698=
XM_011521067.2:c.2151G>A	XP_011519369.1:p.Glu717=
XM_011521069.2:c.2064G>A	XP_011519371.1:p.Glu688=
XM_017020536.2:c.1647G>A	XP_016876025.1:p.Glu549=
XM_017020537.1:c.1329G>A	XP_016876026.1:p.Glu443=
XM_024449336.1:c.2151G>A	XP_024305104.1:p.Glu717=
NM_052867.4:c.2094G>A MANE Select	NP_443099.1:p.Glu698=
NM_001350748.2:c.2094G>A	NP_001337677.1:p.Glu698=
NM_001350749.2:c.2094G>A	NP_001337678.1:p.Glu698=
NM_001350750.2:c.2007G>A	NP_001337679.1:p.Glu669=
NM_001350751.2:c.2007G>A	NP_001337680.1:p.Glu669=