Canonical Allele Identifier: CA2114417640

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101145489A= , CM000675.2:g.101145489A=	GRCh38
NC_000013.10:g.101797840A= , CM000675.1:g.101797840A=	GRCh37
NC_000013.9:g.100595841A=	NCBI36
NG_053176.1:g.276718T=

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.1840-593T= MANE Select	NP_443099.1:n.1840-593T=
ENST00000251127.11:c.1840-593T= MANE Select	ENSP00000251127.6:n.1840-593T=
NM_001350748.1:c.1840-593T=	NP_001337677.1:n.1840-593T=
NM_001350748.2:c.1840-593T=	NP_001337677.1:n.1840-593T=
NM_001350749.1:c.1840-593T=	NP_001337678.1:n.1840-593T=
NM_001350749.2:c.1840-593T=	NP_001337678.1:n.1840-593T=
NM_001350750.1:c.1753-593T=	NP_001337679.1:n.1753-593T=
NM_001350750.2:c.1753-593T=	NP_001337679.1:n.1753-593T=
NM_001350751.1:c.1753-593T=	NP_001337680.1:n.1753-593T=
NM_001350751.2:c.1753-593T=	NP_001337680.1:n.1753-593T=
NM_052867.2:c.1840-593T=	NP_443099.1:n.1840-593T=
NM_052867.3:c.1840-593T=	NP_443099.1:n.1840-593T=
ENST00000251127.10:c.1840-593T=	ENSP00000251127.6:n.1840-593T=
ENST00000467264.2:c.32-593T=
ENST00000497170.5:n.1994-593T=
ENST00000648359.1:c.1840-593T=	ENSP00000497465.1:n.1840-593T=
ENST00000675150.1:c.1840-20808T=	ENSP00000502680.1:n.1840-20808T=
ENST00000675332.1:c.1840-593T=	ENSP00000501955.1:n.1840-593T=
ENST00000675802.1:c.1840-593T=	ENSP00000501818.1:n.1840-593T=
ENST00000676315.1:c.1753-593T=	ENSP00000501603.1:n.1753-593T=
XM_011521067.1:c.1897-593T=	XP_011519369.1:n.1897-593T=
XM_011521067.2:c.1897-593T=	XP_011519369.1:n.1897-593T=
XM_011521068.1:c.1840-593T=	XP_011519370.1:n.1840-593T=
XM_011521069.1:c.1810-593T=	XP_011519371.1:n.1810-593T=
XM_011521069.2:c.1810-593T=	XP_011519371.1:n.1810-593T=
XM_011521070.1:c.1897-20808T=	XP_011519372.1:n.1897-20808T=
XM_017020536.2:c.1393-593T=	XP_016876025.1:n.1393-593T=
XM_017020537.1:c.1075-593T=	XP_016876026.1:n.1075-593T=
XM_024449336.1:c.1897-593T=	XP_024305104.1:n.1897-593T=