Canonical Allele Identifier: CA2114388833

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081546A= , CM000675.2:g.101081546A=	GRCh38
NC_000013.10:g.101733897A= , CM000675.1:g.101733897A=	GRCh37
NC_000013.9:g.100531898A=	NCBI36
NG_053176.1:g.340661T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3866T= MANE Select	ENSP00000251127.6:p.Val1289=
ENST00000648359.1:c.3866T=	ENSP00000497465.1:p.Val1289=
ENST00000675150.1:c.3587T=	ENSP00000502680.1:p.Val1196=
ENST00000675332.1:c.3953T=	ENSP00000501955.1:p.Val1318=
ENST00000676315.1:c.3779T=	ENSP00000501603.1:p.Val1260=
ENST00000251127.10:c.3866T=	ENSP00000251127.6:p.Val1289=
NM_052867.2:c.3866T=	NP_443099.1:p.Val1289=
XM_011521067.1:c.3923T=	XP_011519369.1:p.Val1308=
XM_011521068.1:c.3866T=	XP_011519370.1:p.Val1289=
XM_011521069.1:c.3836T=	XP_011519371.1:p.Val1279=
XM_011521070.1:c.3644T=	XP_011519372.1:p.Val1215=
NM_001350748.1:c.3953T=	NP_001337677.1:p.Val1318=
NM_001350749.1:c.3866T=	NP_001337678.1:p.Val1289=
NM_001350750.1:c.3779T=	NP_001337679.1:p.Val1260=
NM_001350751.1:c.3779T=	NP_001337680.1:p.Val1260=
NM_052867.3:c.3866T=	NP_443099.1:p.Val1289=
XM_011521067.2:c.3923T=	XP_011519369.1:p.Val1308=
XM_011521069.2:c.3836T=	XP_011519371.1:p.Val1279=
XM_017020536.2:c.3419T=	XP_016876025.1:p.Val1140=
XM_017020537.1:c.3101T=	XP_016876026.1:p.Val1034=
XM_024449336.1:c.4010T=	XP_024305104.1:p.Val1337=
NM_052867.4:c.3866T= MANE Select	NP_443099.1:p.Val1289=
NM_001350748.2:c.3953T=	NP_001337677.1:p.Val1318=
NM_001350749.2:c.3866T=	NP_001337678.1:p.Val1289=
NM_001350750.2:c.3779T=	NP_001337679.1:p.Val1260=
NM_001350751.2:c.3779T=	NP_001337680.1:p.Val1260=