Canonical Allele Identifier: CA2114389783

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101083769C= , CM000675.2:g.101083769C=	GRCh38
NC_000013.10:g.101736120C= , CM000675.1:g.101736120C=	GRCh37
NC_000013.9:g.100534121C=	NCBI36
NG_053176.1:g.338438G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3525G= MANE Select	ENSP00000251127.6:p.Trp1175=
ENST00000648359.1:c.3525G=	ENSP00000497465.1:p.Trp1175=
ENST00000675150.1:c.3246G=	ENSP00000502680.1:p.Trp1082=
ENST00000675332.1:c.3612G=	ENSP00000501955.1:p.Trp1204=
ENST00000676315.1:c.3438G=	ENSP00000501603.1:p.Trp1146=
ENST00000251127.10:c.3525G=	ENSP00000251127.6:p.Trp1175=
NM_052867.2:c.3525G=	NP_443099.1:p.Trp1175=
XM_011521067.1:c.3582G=	XP_011519369.1:p.Trp1194=
XM_011521068.1:c.3525G=	XP_011519370.1:p.Trp1175=
XM_011521069.1:c.3495G=	XP_011519371.1:p.Trp1165=
XM_011521070.1:c.3303G=	XP_011519372.1:p.Trp1101=
NM_001350748.1:c.3612G=	NP_001337677.1:p.Trp1204=
NM_001350749.1:c.3525G=	NP_001337678.1:p.Trp1175=
NM_001350750.1:c.3438G=	NP_001337679.1:p.Trp1146=
NM_001350751.1:c.3438G=	NP_001337680.1:p.Trp1146=
NM_052867.3:c.3525G=	NP_443099.1:p.Trp1175=
XM_011521067.2:c.3582G=	XP_011519369.1:p.Trp1194=
XM_011521069.2:c.3495G=	XP_011519371.1:p.Trp1165=
XM_017020536.2:c.3078G=	XP_016876025.1:p.Trp1026=
XM_017020537.1:c.2760G=	XP_016876026.1:p.Trp920=
XM_024449336.1:c.3669G=	XP_024305104.1:p.Trp1223=
NM_052867.4:c.3525G= MANE Select	NP_443099.1:p.Trp1175=
NM_001350748.2:c.3612G=	NP_001337677.1:p.Trp1204=
NM_001350749.2:c.3525G=	NP_001337678.1:p.Trp1175=
NM_001350750.2:c.3438G=	NP_001337679.1:p.Trp1146=
NM_001350751.2:c.3438G=	NP_001337680.1:p.Trp1146=