Canonical Allele Identifier: CA388646342

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101067938T>C , CM000675.2:g.101067938T>C	GRCh38
NC_000013.10:g.101720290T>C , CM000675.1:g.101720290T>C	GRCh37
NC_000013.9:g.100518291T>C	NCBI36
NG_053176.1:g.354269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4426A>G MANE Select	ENSP00000251127.6:p.Met1476Val
ENST00000648359.1:c.4426A>G	ENSP00000497465.1:p.Met1476Val
ENST00000675150.1:c.4147A>G	ENSP00000502680.1:p.Met1383Val
ENST00000675332.1:c.4513A>G	ENSP00000501955.1:p.Met1505Val
ENST00000676315.1:c.4339A>G	ENSP00000501603.1:p.Met1447Val
ENST00000251127.10:c.4426A>G	ENSP00000251127.6:p.Met1476Val
NM_052867.2:c.4426A>G	NP_443099.1:p.Met1476Val
XM_011521067.1:c.4483A>G	XP_011519369.1:p.Met1495Val
XM_011521068.1:c.4426A>G	XP_011519370.1:p.Met1476Val
XM_011521069.1:c.4396A>G	XP_011519371.1:p.Met1466Val
XM_011521070.1:c.4204A>G	XP_011519372.1:p.Met1402Val
NM_001350748.1:c.4513A>G	NP_001337677.1:p.Met1505Val
NM_001350749.1:c.4426A>G	NP_001337678.1:p.Met1476Val
NM_001350750.1:c.4339A>G	NP_001337679.1:p.Met1447Val
NM_001350751.1:c.4339A>G	NP_001337680.1:p.Met1447Val
NM_052867.3:c.4426A>G	NP_443099.1:p.Met1476Val
XM_011521067.2:c.4483A>G	XP_011519369.1:p.Met1495Val
XM_011521069.2:c.4396A>G	XP_011519371.1:p.Met1466Val
XM_017020536.2:c.3979A>G	XP_016876025.1:p.Met1327Val
XM_017020537.1:c.3661A>G	XP_016876026.1:p.Met1221Val
XM_024449336.1:c.4570A>G	XP_024305104.1:p.Met1524Val
NM_052867.4:c.4426A>G MANE Select	NP_443099.1:p.Met1476Val
NM_001350748.2:c.4513A>G	NP_001337677.1:p.Met1505Val
NM_001350749.2:c.4426A>G	NP_001337678.1:p.Met1476Val
NM_001350750.2:c.4339A>G	NP_001337679.1:p.Met1447Val
NM_001350751.2:c.4339A>G	NP_001337680.1:p.Met1447Val