Canonical Allele Identifier: CA2839591086

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081743A>G , CM000675.2:g.101081743A>G	GRCh38
NC_000013.10:g.101734094A>G , CM000675.1:g.101734094A>G	GRCh37
NC_000013.9:g.100532095A>G	NCBI36
NG_053176.1:g.340464T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3766-97T>C MANE Select	ENSP00000251127.6:n.3766-97T>C
ENST00000648359.1:c.3766-97T>C	ENSP00000497465.1:n.3766-97T>C
ENST00000675150.1:c.3487-97T>C	ENSP00000502680.1:n.3487-97T>C
ENST00000675332.1:c.3853-97T>C	ENSP00000501955.1:n.3853-97T>C
ENST00000676315.1:c.3679-97T>C	ENSP00000501603.1:n.3679-97T>C
ENST00000251127.10:c.3766-97T>C	ENSP00000251127.6:n.3766-97T>C
NM_052867.2:c.3766-97T>C	NP_443099.1:n.3766-97T>C
XM_011521067.1:c.3823-97T>C	XP_011519369.1:n.3823-97T>C
XM_011521068.1:c.3766-97T>C	XP_011519370.1:n.3766-97T>C
XM_011521069.1:c.3736-97T>C	XP_011519371.1:n.3736-97T>C
XM_011521070.1:c.3544-97T>C	XP_011519372.1:n.3544-97T>C
NM_001350748.1:c.3853-97T>C	NP_001337677.1:n.3853-97T>C
NM_001350749.1:c.3766-97T>C	NP_001337678.1:n.3766-97T>C
NM_001350750.1:c.3679-97T>C	NP_001337679.1:n.3679-97T>C
NM_001350751.1:c.3679-97T>C	NP_001337680.1:n.3679-97T>C
NM_052867.3:c.3766-97T>C	NP_443099.1:n.3766-97T>C
XM_011521067.2:c.3823-97T>C	XP_011519369.1:n.3823-97T>C
XM_011521069.2:c.3736-97T>C	XP_011519371.1:n.3736-97T>C
XM_017020536.2:c.3319-97T>C	XP_016876025.1:n.3319-97T>C
XM_017020537.1:c.3001-97T>C	XP_016876026.1:n.3001-97T>C
XM_024449336.1:c.3910-97T>C	XP_024305104.1:n.3910-97T>C
NM_052867.4:c.3766-97T>C MANE Select	NP_443099.1:n.3766-97T>C
NM_001350748.2:c.3853-97T>C	NP_001337677.1:n.3853-97T>C
NM_001350749.2:c.3766-97T>C	NP_001337678.1:n.3766-97T>C
NM_001350750.2:c.3679-97T>C	NP_001337679.1:n.3679-97T>C
NM_001350751.2:c.3679-97T>C	NP_001337680.1:n.3679-97T>C