Canonical Allele Identifier: CA2114388846

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081569C= , CM000675.2:g.101081569C=	GRCh38
NC_000013.10:g.101733920C= , CM000675.1:g.101733920C=	GRCh37
NC_000013.9:g.100531921C=	NCBI36
NG_053176.1:g.340638G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3843G= MANE Select	ENSP00000251127.6:p.Thr1281=
ENST00000648359.1:c.3843G=	ENSP00000497465.1:p.Thr1281=
ENST00000675150.1:c.3564G=	ENSP00000502680.1:p.Thr1188=
ENST00000675332.1:c.3930G=	ENSP00000501955.1:p.Thr1310=
ENST00000676315.1:c.3756G=	ENSP00000501603.1:p.Thr1252=
ENST00000251127.10:c.3843G=	ENSP00000251127.6:p.Thr1281=
NM_052867.2:c.3843G=	NP_443099.1:p.Thr1281=
XM_011521067.1:c.3900G=	XP_011519369.1:p.Thr1300=
XM_011521068.1:c.3843G=	XP_011519370.1:p.Thr1281=
XM_011521069.1:c.3813G=	XP_011519371.1:p.Thr1271=
XM_011521070.1:c.3621G=	XP_011519372.1:p.Thr1207=
NM_001350748.1:c.3930G=	NP_001337677.1:p.Thr1310=
NM_001350749.1:c.3843G=	NP_001337678.1:p.Thr1281=
NM_001350750.1:c.3756G=	NP_001337679.1:p.Thr1252=
NM_001350751.1:c.3756G=	NP_001337680.1:p.Thr1252=
NM_052867.3:c.3843G=	NP_443099.1:p.Thr1281=
XM_011521067.2:c.3900G=	XP_011519369.1:p.Thr1300=
XM_011521069.2:c.3813G=	XP_011519371.1:p.Thr1271=
XM_017020536.2:c.3396G=	XP_016876025.1:p.Thr1132=
XM_017020537.1:c.3078G=	XP_016876026.1:p.Thr1026=
XM_024449336.1:c.3987G=	XP_024305104.1:p.Thr1329=
NM_052867.4:c.3843G= MANE Select	NP_443099.1:p.Thr1281=
NM_001350748.2:c.3930G=	NP_001337677.1:p.Thr1310=
NM_001350749.2:c.3843G=	NP_001337678.1:p.Thr1281=
NM_001350750.2:c.3756G=	NP_001337679.1:p.Thr1252=
NM_001350751.2:c.3756G=	NP_001337680.1:p.Thr1252=