Canonical Allele Identifier: CA388704474

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101229522T>C , CM000675.2:g.101229522T>C	GRCh38
NC_000013.10:g.101881873T>C , CM000675.1:g.101881873T>C	GRCh37
NC_000013.9:g.100679874T>C	NCBI36
NG_053176.1:g.192685A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.1497A>G MANE Select	NP_443099.1:p.Ile499Met
ENST00000251127.11:c.1497A>G MANE Select	ENSP00000251127.6:p.Ile499Met
NM_001350748.1:c.1497A>G	NP_001337677.1:p.Ile499Met
NM_001350748.2:c.1497A>G	NP_001337677.1:p.Ile499Met
NM_001350749.1:c.1497A>G	NP_001337678.1:p.Ile499Met
NM_001350749.2:c.1497A>G	NP_001337678.1:p.Ile499Met
NM_001350750.1:c.1410A>G	NP_001337679.1:p.Ile470Met
NM_001350750.2:c.1410A>G	NP_001337679.1:p.Ile470Met
NM_001350751.1:c.1410A>G	NP_001337680.1:p.Ile470Met
NM_001350751.2:c.1410A>G	NP_001337680.1:p.Ile470Met
NM_052867.2:c.1497A>G	NP_443099.1:p.Ile499Met
NM_052867.3:c.1497A>G	NP_443099.1:p.Ile499Met
ENST00000251127.10:c.1497A>G	ENSP00000251127.6:p.Ile499Met
ENST00000470333.1:n.1593A>G
ENST00000497170.5:n.1651A>G
ENST00000648359.1:c.1497A>G	ENSP00000497465.1:p.Ile499Met
ENST00000674840.1:n.1595A>G
ENST00000674904.1:n.1577A>G
ENST00000675150.1:c.1497A>G	ENSP00000502680.1:p.Ile499Met
ENST00000675332.1:c.1497A>G	ENSP00000501955.1:p.Ile499Met
ENST00000675594.1:c.*934A>G	ENSP00000502490.1:n.*934A>G
ENST00000675802.1:c.1497A>G	ENSP00000501818.1:p.Ile499Met
ENST00000676315.1:c.1410A>G	ENSP00000501603.1:p.Ile470Met
ENST00000676439.1:n.1671A>G
XM_011521067.1:c.1554A>G	XP_011519369.1:p.Ile518Met
XM_011521067.2:c.1554A>G	XP_011519369.1:p.Ile518Met
XM_011521068.1:c.1497A>G	XP_011519370.1:p.Ile499Met
XM_011521069.1:c.1467A>G	XP_011519371.1:p.Ile489Met
XM_011521069.2:c.1467A>G	XP_011519371.1:p.Ile489Met
XM_011521070.1:c.1554A>G	XP_011519372.1:p.Ile518Met
XM_017020536.2:c.1050A>G	XP_016876025.1:p.Ile350Met
XM_017020537.1:c.732A>G	XP_016876026.1:p.Ile244Met
XM_024449336.1:c.1554A>G	XP_024305104.1:p.Ile518Met