Canonical Allele Identifier: CA388651905

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101083772T>G , CM000675.2:g.101083772T>G	GRCh38
NC_000013.10:g.101736123T>G , CM000675.1:g.101736123T>G	GRCh37
NC_000013.9:g.100534124T>G	NCBI36
NG_053176.1:g.338435A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.3522A>C MANE Select	NP_443099.1:p.Arg1174Ser
ENST00000251127.11:c.3522A>C MANE Select	ENSP00000251127.6:p.Arg1174Ser
NM_001350748.1:c.3609A>C	NP_001337677.1:p.Arg1203Ser
NM_001350748.2:c.3609A>C	NP_001337677.1:p.Arg1203Ser
NM_001350749.1:c.3522A>C	NP_001337678.1:p.Arg1174Ser
NM_001350749.2:c.3522A>C	NP_001337678.1:p.Arg1174Ser
NM_001350750.1:c.3435A>C	NP_001337679.1:p.Arg1145Ser
NM_001350750.2:c.3435A>C	NP_001337679.1:p.Arg1145Ser
NM_001350751.1:c.3435A>C	NP_001337680.1:p.Arg1145Ser
NM_001350751.2:c.3435A>C	NP_001337680.1:p.Arg1145Ser
NM_052867.2:c.3522A>C	NP_443099.1:p.Arg1174Ser
NM_052867.3:c.3522A>C	NP_443099.1:p.Arg1174Ser
ENST00000251127.10:c.3522A>C	ENSP00000251127.6:p.Arg1174Ser
ENST00000648359.1:c.3522A>C	ENSP00000497465.1:p.Arg1174Ser
ENST00000675150.1:c.3243A>C	ENSP00000502680.1:p.Arg1081Ser
ENST00000675332.1:c.3609A>C	ENSP00000501955.1:p.Arg1203Ser
ENST00000676315.1:c.3435A>C	ENSP00000501603.1:p.Arg1145Ser
XM_011521067.1:c.3579A>C	XP_011519369.1:p.Arg1193Ser
XM_011521067.2:c.3579A>C	XP_011519369.1:p.Arg1193Ser
XM_011521068.1:c.3522A>C	XP_011519370.1:p.Arg1174Ser
XM_011521069.1:c.3492A>C	XP_011519371.1:p.Arg1164Ser
XM_011521069.2:c.3492A>C	XP_011519371.1:p.Arg1164Ser
XM_011521070.1:c.3300A>C	XP_011519372.1:p.Arg1100Ser
XM_017020536.2:c.3075A>C	XP_016876025.1:p.Arg1025Ser
XM_017020537.1:c.2757A>C	XP_016876026.1:p.Arg919Ser
XM_024449336.1:c.3666A>C	XP_024305104.1:p.Arg1222Ser