Canonical Allele Identifier: CA388643813

Gene: NALCN NALCN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101057985G>T , CM000675.2:g.101057985G>T	GRCh38
NC_000013.10:g.101710337G>T , CM000675.1:g.101710337G>T	GRCh37
NC_000013.9:g.100508338G>T	NCBI36
NG_053176.1:g.364222C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.4977C>A (NALCN) MANE Select	NP_443099.1:p.Asp1659Glu
ENST00000251127.11:c.4977C>A (NALCN) MANE Select	ENSP00000251127.6:p.Asp1659Glu
NM_001350748.1:c.5064C>A (NALCN)	NP_001337677.1:p.Asp1688Glu
NM_001350748.2:c.5064C>A (NALCN)	NP_001337677.1:p.Asp1688Glu
NM_001350749.1:c.4977C>A (NALCN)	NP_001337678.1:p.Asp1659Glu
NM_001350749.2:c.4977C>A (NALCN)	NP_001337678.1:p.Asp1659Glu
NM_001350750.1:c.4890C>A (NALCN)	NP_001337679.1:p.Asp1630Glu
NM_001350750.2:c.4890C>A (NALCN)	NP_001337679.1:p.Asp1630Glu
NM_001350751.1:c.4890C>A (NALCN)	NP_001337680.1:p.Asp1630Glu
NM_001350751.2:c.4890C>A (NALCN)	NP_001337680.1:p.Asp1630Glu
NM_052867.2:c.4977C>A (NALCN)	NP_443099.1:p.Asp1659Glu
NM_052867.3:c.4977C>A (NALCN)	NP_443099.1:p.Asp1659Glu
NR_047687.1:n.1545G>T (NALCN-AS1)
ENST00000251127.10:c.4977C>A (NALCN)	ENSP00000251127.6:p.Asp1659Glu
ENST00000648359.1:c.*597C>A (NALCN)	ENSP00000497465.1:n.*597C>A
ENST00000675150.1:c.4698C>A (NALCN)	ENSP00000502680.1:p.Asp1566Glu
ENST00000675332.1:c.5064C>A (NALCN)	ENSP00000501955.1:p.Asp1688Glu
ENST00000676315.1:c.4890C>A (NALCN)	ENSP00000501603.1:p.Asp1630Glu
XM_011521067.1:c.5034C>A (NALCN)	XP_011519369.1:p.Asp1678Glu
XM_011521067.2:c.5034C>A (NALCN)	XP_011519369.1:p.Asp1678Glu
XM_011521068.1:c.4977C>A (NALCN)	XP_011519370.1:p.Asp1659Glu
XM_011521069.1:c.4947C>A (NALCN)	XP_011519371.1:p.Asp1649Glu
XM_011521069.2:c.4947C>A (NALCN)	XP_011519371.1:p.Asp1649Glu
XM_011521070.1:c.4755C>A (NALCN)	XP_011519372.1:p.Asp1585Glu
XM_017020536.2:c.4530C>A (NALCN)	XP_016876025.1:p.Asp1510Glu
XM_017020537.1:c.4212C>A (NALCN)	XP_016876026.1:p.Asp1404Glu
XM_024449336.1:c.5121C>A (NALCN)	XP_024305104.1:p.Asp1707Glu