Canonical Allele Identifier: CA388642874

Gene: NALCN NALCN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101055374C>T , CM000675.2:g.101055374C>T	GRCh38
NC_000013.10:g.101707726C>T , CM000675.1:g.101707726C>T	GRCh37
NC_000013.9:g.100505727C>T	NCBI36
NG_053176.1:g.366833G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.5138G>A (NALCN) MANE Select	NP_443099.1:p.Gly1713Asp
ENST00000251127.11:c.5138G>A (NALCN) MANE Select	ENSP00000251127.6:p.Gly1713Asp
NM_001350748.1:c.5225G>A (NALCN)	NP_001337677.1:p.Gly1742Asp
NM_001350748.2:c.5225G>A (NALCN)	NP_001337677.1:p.Gly1742Asp
NM_001350749.1:c.5138G>A (NALCN)	NP_001337678.1:p.Gly1713Asp
NM_001350749.2:c.5138G>A (NALCN)	NP_001337678.1:p.Gly1713Asp
NM_001350750.1:c.5051G>A (NALCN)	NP_001337679.1:p.Gly1684Asp
NM_001350750.2:c.5051G>A (NALCN)	NP_001337679.1:p.Gly1684Asp
NM_001350751.1:c.5051G>A (NALCN)	NP_001337680.1:p.Gly1684Asp
NM_001350751.2:c.5051G>A (NALCN)	NP_001337680.1:p.Gly1684Asp
NM_052867.2:c.5138G>A (NALCN)	NP_443099.1:p.Gly1713Asp
NM_052867.3:c.5138G>A (NALCN)	NP_443099.1:p.Gly1713Asp
NR_047687.1:n.698C>T (NALCN-AS1)
ENST00000251127.10:c.5138G>A (NALCN)	ENSP00000251127.6:p.Gly1713Asp
ENST00000648359.1:c.*758G>A (NALCN)	ENSP00000497465.1:n.*758G>A
ENST00000675150.1:c.4859G>A (NALCN)	ENSP00000502680.1:p.Gly1620Asp
ENST00000675332.1:c.5225G>A (NALCN)	ENSP00000501955.1:p.Gly1742Asp
ENST00000676315.1:c.5051G>A (NALCN)	ENSP00000501603.1:p.Gly1684Asp
XM_011521067.1:c.5195G>A (NALCN)	XP_011519369.1:p.Gly1732Asp
XM_011521067.2:c.5195G>A (NALCN)	XP_011519369.1:p.Gly1732Asp
XM_011521068.1:c.5138G>A (NALCN)	XP_011519370.1:p.Gly1713Asp
XM_011521069.1:c.5108G>A (NALCN)	XP_011519371.1:p.Gly1703Asp
XM_011521069.2:c.5108G>A (NALCN)	XP_011519371.1:p.Gly1703Asp
XM_011521070.1:c.4916G>A (NALCN)	XP_011519372.1:p.Gly1639Asp
XM_017020536.2:c.4691G>A (NALCN)	XP_016876025.1:p.Gly1564Asp
XM_017020537.1:c.4373G>A (NALCN)	XP_016876026.1:p.Gly1458Asp
XM_024449336.1:c.5282G>A (NALCN)	XP_024305104.1:p.Gly1761Asp