Canonical Allele Identifier: CA7035017

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101059950G>A , CM000675.2:g.101059950G>A	GRCh38
NC_000013.10:g.101712302G>A , CM000675.1:g.101712302G>A	GRCh37
NC_000013.9:g.100510303G>A	NCBI36
NG_053176.1:g.362257C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4773C>T MANE Select	ENSP00000251127.6:p.Cys1591=
ENST00000648359.1:c.*393C>T	ENSP00000497465.1:n.*393C>T
ENST00000675150.1:c.4494C>T	ENSP00000502680.1:p.Cys1498=
ENST00000675332.1:c.4860C>T	ENSP00000501955.1:p.Cys1620=
ENST00000676315.1:c.4686C>T	ENSP00000501603.1:p.Cys1562=
ENST00000251127.10:c.4773C>T	ENSP00000251127.6:p.Cys1591=
NM_052867.2:c.4773C>T	NP_443099.1:p.Cys1591=
XM_011521067.1:c.4830C>T	XP_011519369.1:p.Cys1610=
XM_011521068.1:c.4773C>T	XP_011519370.1:p.Cys1591=
XM_011521069.1:c.4743C>T	XP_011519371.1:p.Cys1581=
XM_011521070.1:c.4551C>T	XP_011519372.1:p.Cys1517=
NM_001350748.1:c.4860C>T	NP_001337677.1:p.Cys1620=
NM_001350749.1:c.4773C>T	NP_001337678.1:p.Cys1591=
NM_001350750.1:c.4686C>T	NP_001337679.1:p.Cys1562=
NM_001350751.1:c.4686C>T	NP_001337680.1:p.Cys1562=
NM_052867.3:c.4773C>T	NP_443099.1:p.Cys1591=
XM_011521067.2:c.4830C>T	XP_011519369.1:p.Cys1610=
XM_011521069.2:c.4743C>T	XP_011519371.1:p.Cys1581=
XM_017020536.2:c.4326C>T	XP_016876025.1:p.Cys1442=
XM_017020537.1:c.4008C>T	XP_016876026.1:p.Cys1336=
XM_024449336.1:c.4917C>T	XP_024305104.1:p.Cys1639=
NM_052867.4:c.4773C>T MANE Select	NP_443099.1:p.Cys1591=
NM_001350748.2:c.4860C>T	NP_001337677.1:p.Cys1620=
NM_001350749.2:c.4773C>T	NP_001337678.1:p.Cys1591=
NM_001350750.2:c.4686C>T	NP_001337679.1:p.Cys1562=
NM_001350751.2:c.4686C>T	NP_001337680.1:p.Cys1562=