Canonical Allele Identifier: CA388653450

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101747968T>C (hg19) ; chr13:g.101095617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101095617T>C , CM000675.2:g.101095617T>C	GRCh38
NC_000013.10:g.101747968T>C , CM000675.1:g.101747968T>C	GRCh37
NC_000013.9:g.100545969T>C	NCBI36
NG_053176.1:g.326590A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3226A>G MANE Select	ENSP00000251127.6:p.Arg1076Gly
ENST00000648359.1:c.3226A>G	ENSP00000497465.1:p.Arg1076Gly
ENST00000675150.1:c.2947A>G	ENSP00000502680.1:p.Arg983Gly
ENST00000675332.1:c.3313A>G	ENSP00000501955.1:p.Arg1105Gly
ENST00000676315.1:c.3139A>G	ENSP00000501603.1:p.Arg1047Gly
ENST00000251127.10:c.3226A>G	ENSP00000251127.6:p.Arg1076Gly
NM_052867.2:c.3226A>G	NP_443099.1:p.Arg1076Gly
XM_011521067.1:c.3283A>G	XP_011519369.1:p.Arg1095Gly
XM_011521068.1:c.3226A>G	XP_011519370.1:p.Arg1076Gly
XM_011521069.1:c.3196A>G	XP_011519371.1:p.Arg1066Gly
XM_011521070.1:c.3004A>G	XP_011519372.1:p.Arg1002Gly
NM_001350748.1:c.3313A>G	NP_001337677.1:p.Arg1105Gly
NM_001350749.1:c.3226A>G	NP_001337678.1:p.Arg1076Gly
NM_001350750.1:c.3139A>G	NP_001337679.1:p.Arg1047Gly
NM_001350751.1:c.3139A>G	NP_001337680.1:p.Arg1047Gly
NM_052867.3:c.3226A>G	NP_443099.1:p.Arg1076Gly
XM_011521067.2:c.3283A>G	XP_011519369.1:p.Arg1095Gly
XM_011521069.2:c.3196A>G	XP_011519371.1:p.Arg1066Gly
XM_017020536.2:c.2779A>G	XP_016876025.1:p.Arg927Gly
XM_017020537.1:c.2461A>G	XP_016876026.1:p.Arg821Gly
XM_024449336.1:c.3370A>G	XP_024305104.1:p.Arg1124Gly
NM_052867.4:c.3226A>G MANE Select	NP_443099.1:p.Arg1076Gly
NM_001350748.2:c.3313A>G	NP_001337677.1:p.Arg1105Gly
NM_001350749.2:c.3226A>G	NP_001337678.1:p.Arg1076Gly
NM_001350750.2:c.3139A>G	NP_001337679.1:p.Arg1047Gly
NM_001350751.2:c.3139A>G	NP_001337680.1:p.Arg1047Gly