Canonical Allele Identifier: CA2114394821

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101095640G= , CM000675.2:g.101095640G=	GRCh38
NC_000013.10:g.101747991G= , CM000675.1:g.101747991G=	GRCh37
NC_000013.9:g.100545992G=	NCBI36
NG_053176.1:g.326567C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3203C= MANE Select	ENSP00000251127.6:p.Ser1068=
ENST00000648359.1:c.3203C=	ENSP00000497465.1:p.Ser1068=
ENST00000675150.1:c.2924C=	ENSP00000502680.1:p.Ser975=
ENST00000675332.1:c.3290C=	ENSP00000501955.1:p.Ser1097=
ENST00000676315.1:c.3116C=	ENSP00000501603.1:p.Ser1039=
ENST00000251127.10:c.3203C=	ENSP00000251127.6:p.Ser1068=
NM_052867.2:c.3203C=	NP_443099.1:p.Ser1068=
XM_011521067.1:c.3260C=	XP_011519369.1:p.Ser1087=
XM_011521068.1:c.3203C=	XP_011519370.1:p.Ser1068=
XM_011521069.1:c.3173C=	XP_011519371.1:p.Ser1058=
XM_011521070.1:c.2981C=	XP_011519372.1:p.Ser994=
NM_001350748.1:c.3290C=	NP_001337677.1:p.Ser1097=
NM_001350749.1:c.3203C=	NP_001337678.1:p.Ser1068=
NM_001350750.1:c.3116C=	NP_001337679.1:p.Ser1039=
NM_001350751.1:c.3116C=	NP_001337680.1:p.Ser1039=
NM_052867.3:c.3203C=	NP_443099.1:p.Ser1068=
XM_011521067.2:c.3260C=	XP_011519369.1:p.Ser1087=
XM_011521069.2:c.3173C=	XP_011519371.1:p.Ser1058=
XM_017020536.2:c.2756C=	XP_016876025.1:p.Ser919=
XM_017020537.1:c.2438C=	XP_016876026.1:p.Ser813=
XM_024449336.1:c.3347C=	XP_024305104.1:p.Ser1116=
NM_052867.4:c.3203C= MANE Select	NP_443099.1:p.Ser1068=
NM_001350748.2:c.3290C=	NP_001337677.1:p.Ser1097=
NM_001350749.2:c.3203C=	NP_001337678.1:p.Ser1068=
NM_001350750.2:c.3116C=	NP_001337679.1:p.Ser1039=
NM_001350751.2:c.3116C=	NP_001337680.1:p.Ser1039=