Canonical Allele Identifier: CA2114388831

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081538A= , CM000675.2:g.101081538A=	GRCh38
NC_000013.10:g.101733889A= , CM000675.1:g.101733889A=	GRCh37
NC_000013.9:g.100531890A=	NCBI36
NG_053176.1:g.340669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3874T= MANE Select	ENSP00000251127.6:p.Phe1292=
ENST00000648359.1:c.3874T=	ENSP00000497465.1:p.Phe1292=
ENST00000675150.1:c.3595T=	ENSP00000502680.1:p.Phe1199=
ENST00000675332.1:c.3961T=	ENSP00000501955.1:p.Phe1321=
ENST00000676315.1:c.3787T=	ENSP00000501603.1:p.Phe1263=
ENST00000251127.10:c.3874T=	ENSP00000251127.6:p.Phe1292=
NM_052867.2:c.3874T=	NP_443099.1:p.Phe1292=
XM_011521067.1:c.3931T=	XP_011519369.1:p.Phe1311=
XM_011521068.1:c.3874T=	XP_011519370.1:p.Phe1292=
XM_011521069.1:c.3844T=	XP_011519371.1:p.Phe1282=
XM_011521070.1:c.3652T=	XP_011519372.1:p.Phe1218=
NM_001350748.1:c.3961T=	NP_001337677.1:p.Phe1321=
NM_001350749.1:c.3874T=	NP_001337678.1:p.Phe1292=
NM_001350750.1:c.3787T=	NP_001337679.1:p.Phe1263=
NM_001350751.1:c.3787T=	NP_001337680.1:p.Phe1263=
NM_052867.3:c.3874T=	NP_443099.1:p.Phe1292=
XM_011521067.2:c.3931T=	XP_011519369.1:p.Phe1311=
XM_011521069.2:c.3844T=	XP_011519371.1:p.Phe1282=
XM_017020536.2:c.3427T=	XP_016876025.1:p.Phe1143=
XM_017020537.1:c.3109T=	XP_016876026.1:p.Phe1037=
XM_024449336.1:c.4018T=	XP_024305104.1:p.Phe1340=
NM_052867.4:c.3874T= MANE Select	NP_443099.1:p.Phe1292=
NM_001350748.2:c.3961T=	NP_001337677.1:p.Phe1321=
NM_001350749.2:c.3874T=	NP_001337678.1:p.Phe1292=
NM_001350750.2:c.3787T=	NP_001337679.1:p.Phe1263=
NM_001350751.2:c.3787T=	NP_001337680.1:p.Phe1263=