Canonical Allele Identifier: CA388644757

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101062119C>G , CM000675.2:g.101062119C>G	GRCh38
NC_000013.10:g.101714471C>G , CM000675.1:g.101714471C>G	GRCh37
NC_000013.9:g.100512472C>G	NCBI36
NG_053176.1:g.360088G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.4605-1G>C MANE Select	NP_443099.1:n.4605-1G>C
ENST00000251127.11:c.4605-1G>C MANE Select	ENSP00000251127.6:n.4605-1G>C
NM_001350748.1:c.4692-1G>C	NP_001337677.1:n.4692-1G>C
NM_001350748.2:c.4692-1G>C	NP_001337677.1:n.4692-1G>C
NM_001350749.1:c.4605-1G>C	NP_001337678.1:n.4605-1G>C
NM_001350749.2:c.4605-1G>C	NP_001337678.1:n.4605-1G>C
NM_001350750.1:c.4518-1G>C	NP_001337679.1:n.4518-1G>C
NM_001350750.2:c.4518-1G>C	NP_001337679.1:n.4518-1G>C
NM_001350751.1:c.4518-1G>C	NP_001337680.1:n.4518-1G>C
NM_001350751.2:c.4518-1G>C	NP_001337680.1:n.4518-1G>C
NM_052867.2:c.4605-1G>C	NP_443099.1:n.4605-1G>C
NM_052867.3:c.4605-1G>C	NP_443099.1:n.4605-1G>C
ENST00000251127.10:c.4605-1G>C	ENSP00000251127.6:n.4605-1G>C
ENST00000648359.1:c.*225-1G>C	ENSP00000497465.1:n.*225-1G>C
ENST00000675150.1:c.4326-1G>C	ENSP00000502680.1:n.4326-1G>C
ENST00000675332.1:c.4692-1G>C	ENSP00000501955.1:n.4692-1G>C
ENST00000676315.1:c.4518-1G>C	ENSP00000501603.1:n.4518-1G>C
XM_011521067.1:c.4662-1G>C	XP_011519369.1:n.4662-1G>C
XM_011521067.2:c.4662-1G>C	XP_011519369.1:n.4662-1G>C
XM_011521068.1:c.4605-1G>C	XP_011519370.1:n.4605-1G>C
XM_011521069.1:c.4575-1G>C	XP_011519371.1:n.4575-1G>C
XM_011521069.2:c.4575-1G>C	XP_011519371.1:n.4575-1G>C
XM_011521070.1:c.4383-1G>C	XP_011519372.1:n.4383-1G>C
XM_017020536.2:c.4158-1G>C	XP_016876025.1:n.4158-1G>C
XM_017020537.1:c.3840-1G>C	XP_016876026.1:n.3840-1G>C
XM_024449336.1:c.4749-1G>C	XP_024305104.1:n.4749-1G>C