Canonical Allele Identifier: CA388651715

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101083717G>A , CM000675.2:g.101083717G>A	GRCh38
NC_000013.10:g.101736068G>A , CM000675.1:g.101736068G>A	GRCh37
NC_000013.9:g.100534069G>A	NCBI36
NG_053176.1:g.338490C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_052867.4:c.3577C>T MANE Select	NP_443099.1:p.Arg1193Cys
ENST00000251127.11:c.3577C>T MANE Select	ENSP00000251127.6:p.Arg1193Cys
NM_001350748.1:c.3664C>T	NP_001337677.1:p.Arg1222Cys
NM_001350748.2:c.3664C>T	NP_001337677.1:p.Arg1222Cys
NM_001350749.1:c.3577C>T	NP_001337678.1:p.Arg1193Cys
NM_001350749.2:c.3577C>T	NP_001337678.1:p.Arg1193Cys
NM_001350750.1:c.3490C>T	NP_001337679.1:p.Arg1164Cys
NM_001350750.2:c.3490C>T	NP_001337679.1:p.Arg1164Cys
NM_001350751.1:c.3490C>T	NP_001337680.1:p.Arg1164Cys
NM_001350751.2:c.3490C>T	NP_001337680.1:p.Arg1164Cys
NM_052867.2:c.3577C>T	NP_443099.1:p.Arg1193Cys
NM_052867.3:c.3577C>T	NP_443099.1:p.Arg1193Cys
ENST00000251127.10:c.3577C>T	ENSP00000251127.6:p.Arg1193Cys
ENST00000648359.1:c.3577C>T	ENSP00000497465.1:p.Arg1193Cys
ENST00000675150.1:c.3298C>T	ENSP00000502680.1:p.Arg1100Cys
ENST00000675332.1:c.3664C>T	ENSP00000501955.1:p.Arg1222Cys
ENST00000676315.1:c.3490C>T	ENSP00000501603.1:p.Arg1164Cys
XM_011521067.1:c.3634C>T	XP_011519369.1:p.Arg1212Cys
XM_011521067.2:c.3634C>T	XP_011519369.1:p.Arg1212Cys
XM_011521068.1:c.3577C>T	XP_011519370.1:p.Arg1193Cys
XM_011521069.1:c.3547C>T	XP_011519371.1:p.Arg1183Cys
XM_011521069.2:c.3547C>T	XP_011519371.1:p.Arg1183Cys
XM_011521070.1:c.3355C>T	XP_011519372.1:p.Arg1119Cys
XM_017020536.2:c.3130C>T	XP_016876025.1:p.Arg1044Cys
XM_017020537.1:c.2812C>T	XP_016876026.1:p.Arg938Cys
XM_024449336.1:c.3721C>T	XP_024305104.1:p.Arg1241Cys