Canonical Allele Identifier: CA2114388809

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081485A= , CM000675.2:g.101081485A=	GRCh38
NC_000013.10:g.101733836A= , CM000675.1:g.101733836A=	GRCh37
NC_000013.9:g.100531837A=	NCBI36
NG_053176.1:g.340722T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3885+42T= MANE Select	ENSP00000251127.6:n.3885+42T=
ENST00000648359.1:c.3885+42T=	ENSP00000497465.1:n.3885+42T=
ENST00000675150.1:c.3606+42T=	ENSP00000502680.1:n.3606+42T=
ENST00000675332.1:c.3972+42T=	ENSP00000501955.1:n.3972+42T=
ENST00000676315.1:c.3798+42T=	ENSP00000501603.1:n.3798+42T=
ENST00000251127.10:c.3885+42T=	ENSP00000251127.6:n.3885+42T=
NM_052867.2:c.3885+42T=	NP_443099.1:n.3885+42T=
XM_011521067.1:c.3942+42T=	XP_011519369.1:n.3942+42T=
XM_011521068.1:c.3885+42T=	XP_011519370.1:n.3885+42T=
XM_011521069.1:c.3855+42T=	XP_011519371.1:n.3855+42T=
XM_011521070.1:c.3663+42T=	XP_011519372.1:n.3663+42T=
NM_001350748.1:c.3972+42T=	NP_001337677.1:n.3972+42T=
NM_001350749.1:c.3885+42T=	NP_001337678.1:n.3885+42T=
NM_001350750.1:c.3798+42T=	NP_001337679.1:n.3798+42T=
NM_001350751.1:c.3798+42T=	NP_001337680.1:n.3798+42T=
NM_052867.3:c.3885+42T=	NP_443099.1:n.3885+42T=
XM_011521067.2:c.3942+42T=	XP_011519369.1:n.3942+42T=
XM_011521069.2:c.3855+42T=	XP_011519371.1:n.3855+42T=
XM_017020536.2:c.3438+42T=	XP_016876025.1:n.3438+42T=
XM_017020537.1:c.3120+42T=	XP_016876026.1:n.3120+42T=
XM_024449336.1:c.4029+42T=	XP_024305104.1:n.4029+42T=
NM_052867.4:c.3885+42T= MANE Select	NP_443099.1:n.3885+42T=
NM_001350748.2:c.3972+42T=	NP_001337677.1:n.3972+42T=
NM_001350749.2:c.3885+42T=	NP_001337678.1:n.3885+42T=
NM_001350750.2:c.3798+42T=	NP_001337679.1:n.3798+42T=
NM_001350751.2:c.3798+42T=	NP_001337680.1:n.3798+42T=