Canonical Allele Identifier: CA2114483864

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292072A= , CM000675.2:g.101292072A=	GRCh38
NC_000013.10:g.101944423A= , CM000675.1:g.101944423A=	GRCh37
NC_000013.9:g.100742424A=	NCBI36
NG_053176.1:g.130135T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.965T= MANE Select	ENSP00000251127.6:p.Ile322=
ENST00000648359.1:c.965T=	ENSP00000497465.1:p.Ile322=
ENST00000674840.1:n.1063T=
ENST00000674904.1:n.1045T=
ENST00000675075.1:n.567T=
ENST00000675150.1:c.965T=	ENSP00000502680.1:p.Ile322=
ENST00000675332.1:c.965T=	ENSP00000501955.1:p.Ile322=
ENST00000675415.1:n.1148T=
ENST00000675594.1:c.*402T=	ENSP00000502490.1:n.*402T=
ENST00000675802.1:c.965T=	ENSP00000501818.1:p.Ile322=
ENST00000676315.1:c.965T=	ENSP00000501603.1:p.Ile322=
ENST00000676439.1:n.1139T=
ENST00000251127.10:c.965T=	ENSP00000251127.6:p.Ile322=
ENST00000470333.1:n.1061T=
ENST00000497170.5:n.1119T=
NM_052867.2:c.965T=	NP_443099.1:p.Ile322=
XM_011521067.1:c.1022T=	XP_011519369.1:p.Ile341=
XM_011521068.1:c.965T=	XP_011519370.1:p.Ile322=
XM_011521069.1:c.1022T=	XP_011519371.1:p.Ile341=
XM_011521070.1:c.1022T=	XP_011519372.1:p.Ile341=
NM_001350748.1:c.965T=	NP_001337677.1:p.Ile322=
NM_001350749.1:c.965T=	NP_001337678.1:p.Ile322=
NM_001350750.1:c.965T=	NP_001337679.1:p.Ile322=
NM_001350751.1:c.965T=	NP_001337680.1:p.Ile322=
NM_052867.3:c.965T=	NP_443099.1:p.Ile322=
XM_011521067.2:c.1022T=	XP_011519369.1:p.Ile341=
XM_011521069.2:c.1022T=	XP_011519371.1:p.Ile341=
XM_017020536.2:c.518T=	XP_016876025.1:p.Ile173=
XM_017020537.1:c.200T=	XP_016876026.1:p.Ile67=
XM_024449336.1:c.1022T=	XP_024305104.1:p.Ile341=
NM_052867.4:c.965T= MANE Select	NP_443099.1:p.Ile322=
NM_001350748.2:c.965T=	NP_001337677.1:p.Ile322=
NM_001350749.2:c.965T=	NP_001337678.1:p.Ile322=
NM_001350750.2:c.965T=	NP_001337679.1:p.Ile322=
NM_001350751.2:c.965T=	NP_001337680.1:p.Ile322=