Canonical Allele Identifier: CA2114483844

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101291992G= , CM000675.2:g.101291992G=	GRCh38
NC_000013.10:g.101944343G= , CM000675.1:g.101944343G=	GRCh37
NC_000013.9:g.100742344G=	NCBI36
NG_053176.1:g.130215C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.1045C= MANE Select	ENSP00000251127.6:p.Gln349=
ENST00000648359.1:c.1045C=	ENSP00000497465.1:p.Gln349=
ENST00000674840.1:n.1143C=
ENST00000674904.1:n.1125C=
ENST00000675150.1:c.1045C=	ENSP00000502680.1:p.Gln349=
ENST00000675332.1:c.1045C=	ENSP00000501955.1:p.Gln349=
ENST00000675415.1:n.1228C=
ENST00000675594.1:c.*482C=	ENSP00000502490.1:n.*482C=
ENST00000675802.1:c.1045C=	ENSP00000501818.1:p.Gln349=
ENST00000676315.1:c.1045C=	ENSP00000501603.1:p.Gln349=
ENST00000676439.1:n.1219C=
ENST00000251127.10:c.1045C=	ENSP00000251127.6:p.Gln349=
ENST00000470333.1:n.1141C=
ENST00000497170.5:n.1199C=
NM_052867.2:c.1045C=	NP_443099.1:p.Gln349=
XM_011521067.1:c.1102C=	XP_011519369.1:p.Gln368=
XM_011521068.1:c.1045C=	XP_011519370.1:p.Gln349=
XM_011521069.1:c.1102C=	XP_011519371.1:p.Gln368=
XM_011521070.1:c.1102C=	XP_011519372.1:p.Gln368=
NM_001350748.1:c.1045C=	NP_001337677.1:p.Gln349=
NM_001350749.1:c.1045C=	NP_001337678.1:p.Gln349=
NM_001350750.1:c.1045C=	NP_001337679.1:p.Gln349=
NM_001350751.1:c.1045C=	NP_001337680.1:p.Gln349=
NM_052867.3:c.1045C=	NP_443099.1:p.Gln349=
XM_011521067.2:c.1102C=	XP_011519369.1:p.Gln368=
XM_011521069.2:c.1102C=	XP_011519371.1:p.Gln368=
XM_017020536.2:c.598C=	XP_016876025.1:p.Gln200=
XM_017020537.1:c.280C=	XP_016876026.1:p.Gln94=
XM_024449336.1:c.1102C=	XP_024305104.1:p.Gln368=
NM_052867.4:c.1045C= MANE Select	NP_443099.1:p.Gln349=
NM_001350748.2:c.1045C=	NP_001337677.1:p.Gln349=
NM_001350749.2:c.1045C=	NP_001337678.1:p.Gln349=
NM_001350750.2:c.1045C=	NP_001337679.1:p.Gln349=
NM_001350751.2:c.1045C=	NP_001337680.1:p.Gln349=