Canonical Allele Identifier: CA7034995

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101059808G>A , CM000675.2:g.101059808G>A	GRCh38
NC_000013.10:g.101712160G>A , CM000675.1:g.101712160G>A	GRCh37
NC_000013.9:g.100510161G>A	NCBI36
NG_053176.1:g.362399C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4905+10C>T MANE Select	ENSP00000251127.6:n.4905+10C>T
ENST00000648359.1:c.*525+10C>T	ENSP00000497465.1:n.*525+10C>T
ENST00000675150.1:c.4626+10C>T	ENSP00000502680.1:n.4626+10C>T
ENST00000675332.1:c.4992+10C>T	ENSP00000501955.1:n.4992+10C>T
ENST00000676315.1:c.4818+10C>T	ENSP00000501603.1:n.4818+10C>T
ENST00000251127.10:c.4905+10C>T	ENSP00000251127.6:n.4905+10C>T
NM_052867.2:c.4905+10C>T	NP_443099.1:n.4905+10C>T
XM_011521067.1:c.4962+10C>T	XP_011519369.1:n.4962+10C>T
XM_011521068.1:c.4905+10C>T	XP_011519370.1:n.4905+10C>T
XM_011521069.1:c.4875+10C>T	XP_011519371.1:n.4875+10C>T
XM_011521070.1:c.4683+10C>T	XP_011519372.1:n.4683+10C>T
NM_001350748.1:c.4992+10C>T	NP_001337677.1:n.4992+10C>T
NM_001350749.1:c.4905+10C>T	NP_001337678.1:n.4905+10C>T
NM_001350750.1:c.4818+10C>T	NP_001337679.1:n.4818+10C>T
NM_001350751.1:c.4818+10C>T	NP_001337680.1:n.4818+10C>T
NM_052867.3:c.4905+10C>T	NP_443099.1:n.4905+10C>T
XM_011521067.2:c.4962+10C>T	XP_011519369.1:n.4962+10C>T
XM_011521069.2:c.4875+10C>T	XP_011519371.1:n.4875+10C>T
XM_017020536.2:c.4458+10C>T	XP_016876025.1:n.4458+10C>T
XM_017020537.1:c.4140+10C>T	XP_016876026.1:n.4140+10C>T
XM_024449336.1:c.5049+10C>T	XP_024305104.1:n.5049+10C>T
NM_052867.4:c.4905+10C>T MANE Select	NP_443099.1:n.4905+10C>T
NM_001350748.2:c.4992+10C>T	NP_001337677.1:n.4992+10C>T
NM_001350749.2:c.4905+10C>T	NP_001337678.1:n.4905+10C>T
NM_001350750.2:c.4818+10C>T	NP_001337679.1:n.4818+10C>T
NM_001350751.2:c.4818+10C>T	NP_001337680.1:n.4818+10C>T