Canonical Allele Identifier: CA2114483863

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292071A= , CM000675.2:g.101292071A=	GRCh38
NC_000013.10:g.101944422A= , CM000675.1:g.101944422A=	GRCh37
NC_000013.9:g.100742423A=	NCBI36
NG_053176.1:g.130136T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.966T= MANE Select	ENSP00000251127.6:p.Ile322=
ENST00000648359.1:c.966T=	ENSP00000497465.1:p.Ile322=
ENST00000674840.1:n.1064T=
ENST00000674904.1:n.1046T=
ENST00000675075.1:n.568T=
ENST00000675150.1:c.966T=	ENSP00000502680.1:p.Ile322=
ENST00000675332.1:c.966T=	ENSP00000501955.1:p.Ile322=
ENST00000675415.1:n.1149T=
ENST00000675594.1:c.*403T=	ENSP00000502490.1:n.*403T=
ENST00000675802.1:c.966T=	ENSP00000501818.1:p.Ile322=
ENST00000676315.1:c.966T=	ENSP00000501603.1:p.Ile322=
ENST00000676439.1:n.1140T=
ENST00000251127.10:c.966T=	ENSP00000251127.6:p.Ile322=
ENST00000470333.1:n.1062T=
ENST00000497170.5:n.1120T=
NM_052867.2:c.966T=	NP_443099.1:p.Ile322=
XM_011521067.1:c.1023T=	XP_011519369.1:p.Ile341=
XM_011521068.1:c.966T=	XP_011519370.1:p.Ile322=
XM_011521069.1:c.1023T=	XP_011519371.1:p.Ile341=
XM_011521070.1:c.1023T=	XP_011519372.1:p.Ile341=
NM_001350748.1:c.966T=	NP_001337677.1:p.Ile322=
NM_001350749.1:c.966T=	NP_001337678.1:p.Ile322=
NM_001350750.1:c.966T=	NP_001337679.1:p.Ile322=
NM_001350751.1:c.966T=	NP_001337680.1:p.Ile322=
NM_052867.3:c.966T=	NP_443099.1:p.Ile322=
XM_011521067.2:c.1023T=	XP_011519369.1:p.Ile341=
XM_011521069.2:c.1023T=	XP_011519371.1:p.Ile341=
XM_017020536.2:c.519T=	XP_016876025.1:p.Ile173=
XM_017020537.1:c.201T=	XP_016876026.1:p.Ile67=
XM_024449336.1:c.1023T=	XP_024305104.1:p.Ile341=
NM_052867.4:c.966T= MANE Select	NP_443099.1:p.Ile322=
NM_001350748.2:c.966T=	NP_001337677.1:p.Ile322=
NM_001350749.2:c.966T=	NP_001337678.1:p.Ile322=
NM_001350750.2:c.966T=	NP_001337679.1:p.Ile322=
NM_001350751.2:c.966T=	NP_001337680.1:p.Ile322=