Canonical Allele Identifier: CA7034916

Gene: NALCN NALCN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101055414C>T , CM000675.2:g.101055414C>T	GRCh38
NC_000013.10:g.101707766C>T , CM000675.1:g.101707766C>T	GRCh37
NC_000013.9:g.100505767C>T	NCBI36
NG_053176.1:g.366793G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.5098G>A (NALCN) MANE Select	ENSP00000251127.6:p.Val1700Met
ENST00000648359.1:c.*718G>A (NALCN)	ENSP00000497465.1:n.*718G>A
ENST00000675150.1:c.4819G>A (NALCN)	ENSP00000502680.1:p.Val1607Met
ENST00000675332.1:c.5185G>A (NALCN)	ENSP00000501955.1:p.Val1729Met
ENST00000676315.1:c.5011G>A (NALCN)	ENSP00000501603.1:p.Val1671Met
ENST00000251127.10:c.5098G>A (NALCN)	ENSP00000251127.6:p.Val1700Met
NM_052867.2:c.5098G>A (NALCN)	NP_443099.1:p.Val1700Met
NR_047687.1:n.738C>T (NALCN-AS1)
XM_011521067.1:c.5155G>A (NALCN)	XP_011519369.1:p.Val1719Met
XM_011521068.1:c.5098G>A (NALCN)	XP_011519370.1:p.Val1700Met
XM_011521069.1:c.5068G>A (NALCN)	XP_011519371.1:p.Val1690Met
XM_011521070.1:c.4876G>A (NALCN)	XP_011519372.1:p.Val1626Met
NM_001350748.1:c.5185G>A (NALCN)	NP_001337677.1:p.Val1729Met
NM_001350749.1:c.5098G>A (NALCN)	NP_001337678.1:p.Val1700Met
NM_001350750.1:c.5011G>A (NALCN)	NP_001337679.1:p.Val1671Met
NM_001350751.1:c.5011G>A (NALCN)	NP_001337680.1:p.Val1671Met
NM_052867.3:c.5098G>A (NALCN)	NP_443099.1:p.Val1700Met
XM_011521067.2:c.5155G>A (NALCN)	XP_011519369.1:p.Val1719Met
XM_011521069.2:c.5068G>A (NALCN)	XP_011519371.1:p.Val1690Met
XM_017020536.2:c.4651G>A (NALCN)	XP_016876025.1:p.Val1551Met
XM_017020537.1:c.4333G>A (NALCN)	XP_016876026.1:p.Val1445Met
XM_024449336.1:c.5242G>A (NALCN)	XP_024305104.1:p.Val1748Met
NM_052867.4:c.5098G>A (NALCN) MANE Select	NP_443099.1:p.Val1700Met
NM_001350748.2:c.5185G>A (NALCN)	NP_001337677.1:p.Val1729Met
NM_001350749.2:c.5098G>A (NALCN)	NP_001337678.1:p.Val1700Met
NM_001350750.2:c.5011G>A (NALCN)	NP_001337679.1:p.Val1671Met
NM_001350751.2:c.5011G>A (NALCN)	NP_001337680.1:p.Val1671Met