Canonical Allele Identifier: CA2114379348

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101061021A= , CM000675.2:g.101061021A=	GRCh38
NC_000013.10:g.101713373A= , CM000675.1:g.101713373A=	GRCh37
NC_000013.9:g.100511374A=	NCBI36
NG_053176.1:g.361186T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.4755+947T= MANE Select	ENSP00000251127.6:n.4755+947T=
ENST00000648359.1:c.*375+947T=	ENSP00000497465.1:n.*375+947T=
ENST00000675150.1:c.4476+947T=	ENSP00000502680.1:n.4476+947T=
ENST00000675332.1:c.4842+947T=	ENSP00000501955.1:n.4842+947T=
ENST00000676315.1:c.4668+947T=	ENSP00000501603.1:n.4668+947T=
ENST00000251127.10:c.4755+947T=	ENSP00000251127.6:n.4755+947T=
NM_052867.2:c.4755+947T=	NP_443099.1:n.4755+947T=
XM_011521067.1:c.4812+947T=	XP_011519369.1:n.4812+947T=
XM_011521068.1:c.4755+947T=	XP_011519370.1:n.4755+947T=
XM_011521069.1:c.4725+947T=	XP_011519371.1:n.4725+947T=
XM_011521070.1:c.4533+947T=	XP_011519372.1:n.4533+947T=
NM_001350748.1:c.4842+947T=	NP_001337677.1:n.4842+947T=
NM_001350749.1:c.4755+947T=	NP_001337678.1:n.4755+947T=
NM_001350750.1:c.4668+947T=	NP_001337679.1:n.4668+947T=
NM_001350751.1:c.4668+947T=	NP_001337680.1:n.4668+947T=
NM_052867.3:c.4755+947T=	NP_443099.1:n.4755+947T=
XM_011521067.2:c.4812+947T=	XP_011519369.1:n.4812+947T=
XM_011521069.2:c.4725+947T=	XP_011519371.1:n.4725+947T=
XM_017020536.2:c.4308+947T=	XP_016876025.1:n.4308+947T=
XM_017020537.1:c.3990+947T=	XP_016876026.1:n.3990+947T=
XM_024449336.1:c.4899+947T=	XP_024305104.1:n.4899+947T=
NM_052867.4:c.4755+947T= MANE Select	NP_443099.1:n.4755+947T=
NM_001350748.2:c.4842+947T=	NP_001337677.1:n.4842+947T=
NM_001350749.2:c.4755+947T=	NP_001337678.1:n.4755+947T=
NM_001350750.2:c.4668+947T=	NP_001337679.1:n.4668+947T=
NM_001350751.2:c.4668+947T=	NP_001337680.1:n.4668+947T=