Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101055879G= , CM000675.2:g.101055879G=	GRCh38
NC_000013.10:g.101708231G= , CM000675.1:g.101708231G=	GRCh37
NC_000013.9:g.100506232G=	NCBI36
NG_053176.1:g.366328C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.5024-391C= (NALCN) MANE Select	ENSP00000251127.6:n.5024-391C=
ENST00000648359.1:c.*644-391C= (NALCN)	ENSP00000497465.1:n.*644-391C=
ENST00000675150.1:c.4745-391C= (NALCN)	ENSP00000502680.1:n.4745-391C=
ENST00000675332.1:c.5111-391C= (NALCN)	ENSP00000501955.1:n.5111-391C=
ENST00000676315.1:c.4937-391C= (NALCN)	ENSP00000501603.1:n.4937-391C=
ENST00000251127.10:c.5024-391C= (NALCN)	ENSP00000251127.6:n.5024-391C=
NM_052867.2:c.5024-391C= (NALCN)	NP_443099.1:n.5024-391C=
NR_047687.1:n.770+433G= (NALCN-AS1)
XM_011521067.1:c.5081-391C= (NALCN)	XP_011519369.1:n.5081-391C=
XM_011521068.1:c.5024-391C= (NALCN)	XP_011519370.1:n.5024-391C=
XM_011521069.1:c.4994-391C= (NALCN)	XP_011519371.1:n.4994-391C=
XM_011521070.1:c.4802-391C= (NALCN)	XP_011519372.1:n.4802-391C=
NM_001350748.1:c.5111-391C= (NALCN)	NP_001337677.1:n.5111-391C=
NM_001350749.1:c.5024-391C= (NALCN)	NP_001337678.1:n.5024-391C=
NM_001350750.1:c.4937-391C= (NALCN)	NP_001337679.1:n.4937-391C=
NM_001350751.1:c.4937-391C= (NALCN)	NP_001337680.1:n.4937-391C=
NM_052867.3:c.5024-391C= (NALCN)	NP_443099.1:n.5024-391C=
XM_011521067.2:c.5081-391C= (NALCN)	XP_011519369.1:n.5081-391C=
XM_011521069.2:c.4994-391C= (NALCN)	XP_011519371.1:n.4994-391C=
XM_017020536.2:c.4577-391C= (NALCN)	XP_016876025.1:n.4577-391C=
XM_017020537.1:c.4259-391C= (NALCN)	XP_016876026.1:n.4259-391C=
XM_024449336.1:c.5168-391C= (NALCN)	XP_024305104.1:n.5168-391C=
NM_052867.4:c.5024-391C= (NALCN) MANE Select	NP_443099.1:n.5024-391C=
NM_001350748.2:c.5111-391C= (NALCN)	NP_001337677.1:n.5111-391C=
NM_001350749.2:c.5024-391C= (NALCN)	NP_001337678.1:n.5024-391C=
NM_001350750.2:c.4937-391C= (NALCN)	NP_001337679.1:n.4937-391C=
NM_001350751.2:c.4937-391C= (NALCN)	NP_001337680.1:n.4937-391C=