Canonical Allele Identifier: CA2114388839

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081556C= , CM000675.2:g.101081556C=	GRCh38
NC_000013.10:g.101733907C= , CM000675.1:g.101733907C=	GRCh37
NC_000013.9:g.100531908C=	NCBI36
NG_053176.1:g.340651G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3856G= MANE Select	ENSP00000251127.6:p.Val1286=
ENST00000648359.1:c.3856G=	ENSP00000497465.1:p.Val1286=
ENST00000675150.1:c.3577G=	ENSP00000502680.1:p.Val1193=
ENST00000675332.1:c.3943G=	ENSP00000501955.1:p.Val1315=
ENST00000676315.1:c.3769G=	ENSP00000501603.1:p.Val1257=
ENST00000251127.10:c.3856G=	ENSP00000251127.6:p.Val1286=
NM_052867.2:c.3856G=	NP_443099.1:p.Val1286=
XM_011521067.1:c.3913G=	XP_011519369.1:p.Val1305=
XM_011521068.1:c.3856G=	XP_011519370.1:p.Val1286=
XM_011521069.1:c.3826G=	XP_011519371.1:p.Val1276=
XM_011521070.1:c.3634G=	XP_011519372.1:p.Val1212=
NM_001350748.1:c.3943G=	NP_001337677.1:p.Val1315=
NM_001350749.1:c.3856G=	NP_001337678.1:p.Val1286=
NM_001350750.1:c.3769G=	NP_001337679.1:p.Val1257=
NM_001350751.1:c.3769G=	NP_001337680.1:p.Val1257=
NM_052867.3:c.3856G=	NP_443099.1:p.Val1286=
XM_011521067.2:c.3913G=	XP_011519369.1:p.Val1305=
XM_011521069.2:c.3826G=	XP_011519371.1:p.Val1276=
XM_017020536.2:c.3409G=	XP_016876025.1:p.Val1137=
XM_017020537.1:c.3091G=	XP_016876026.1:p.Val1031=
XM_024449336.1:c.4000G=	XP_024305104.1:p.Val1334=
NM_052867.4:c.3856G= MANE Select	NP_443099.1:p.Val1286=
NM_001350748.2:c.3943G=	NP_001337677.1:p.Val1315=
NM_001350749.2:c.3856G=	NP_001337678.1:p.Val1286=
NM_001350750.2:c.3769G=	NP_001337679.1:p.Val1257=
NM_001350751.2:c.3769G=	NP_001337680.1:p.Val1257=