Canonical Allele Identifier: CA388649672

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101075884A>C , CM000675.2:g.101075884A>C	GRCh38
NC_000013.10:g.101728235A>C , CM000675.1:g.101728235A>C	GRCh37
NC_000013.9:g.100526236A>C	NCBI36
NG_053176.1:g.346323T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.3943T>G MANE Select	NP_443099.1:p.Cys1315Gly
ENST00000251127.11:c.3943T>G MANE Select	ENSP00000251127.6:p.Cys1315Gly
NM_001350748.1:c.4030T>G	NP_001337677.1:p.Cys1344Gly
NM_001350748.2:c.4030T>G	NP_001337677.1:p.Cys1344Gly
NM_001350749.1:c.3943T>G	NP_001337678.1:p.Cys1315Gly
NM_001350749.2:c.3943T>G	NP_001337678.1:p.Cys1315Gly
NM_001350750.1:c.3856T>G	NP_001337679.1:p.Cys1286Gly
NM_001350750.2:c.3856T>G	NP_001337679.1:p.Cys1286Gly
NM_001350751.1:c.3856T>G	NP_001337680.1:p.Cys1286Gly
NM_001350751.2:c.3856T>G	NP_001337680.1:p.Cys1286Gly
NM_052867.2:c.3943T>G	NP_443099.1:p.Cys1315Gly
NM_052867.3:c.3943T>G	NP_443099.1:p.Cys1315Gly
ENST00000251127.10:c.3943T>G	ENSP00000251127.6:p.Cys1315Gly
ENST00000648359.1:c.3943T>G	ENSP00000497465.1:p.Cys1315Gly
ENST00000675150.1:c.3664T>G	ENSP00000502680.1:p.Cys1222Gly
ENST00000675332.1:c.4030T>G	ENSP00000501955.1:p.Cys1344Gly
ENST00000676315.1:c.3856T>G	ENSP00000501603.1:p.Cys1286Gly
XM_011521067.1:c.4000T>G	XP_011519369.1:p.Cys1334Gly
XM_011521067.2:c.4000T>G	XP_011519369.1:p.Cys1334Gly
XM_011521068.1:c.3943T>G	XP_011519370.1:p.Cys1315Gly
XM_011521069.1:c.3913T>G	XP_011519371.1:p.Cys1305Gly
XM_011521069.2:c.3913T>G	XP_011519371.1:p.Cys1305Gly
XM_011521070.1:c.3721T>G	XP_011519372.1:p.Cys1241Gly
XM_017020536.2:c.3496T>G	XP_016876025.1:p.Cys1166Gly
XM_017020537.1:c.3178T>G	XP_016876026.1:p.Cys1060Gly
XM_024449336.1:c.4087T>G	XP_024305104.1:p.Cys1363Gly