Canonical Allele Identifier: CA388650388

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733960A>C (hg19) ; chr13:g.101081609A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081609A>C , CM000675.2:g.101081609A>C	GRCh38
NC_000013.10:g.101733960A>C , CM000675.1:g.101733960A>C	GRCh37
NC_000013.9:g.100531961A>C	NCBI36
NG_053176.1:g.340598T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3803T>G MANE Select	ENSP00000251127.6:p.Phe1268Cys
ENST00000648359.1:c.3803T>G	ENSP00000497465.1:p.Phe1268Cys
ENST00000675150.1:c.3524T>G	ENSP00000502680.1:p.Phe1175Cys
ENST00000675332.1:c.3890T>G	ENSP00000501955.1:p.Phe1297Cys
ENST00000676315.1:c.3716T>G	ENSP00000501603.1:p.Phe1239Cys
ENST00000251127.10:c.3803T>G	ENSP00000251127.6:p.Phe1268Cys
NM_052867.2:c.3803T>G	NP_443099.1:p.Phe1268Cys
XM_011521067.1:c.3860T>G	XP_011519369.1:p.Phe1287Cys
XM_011521068.1:c.3803T>G	XP_011519370.1:p.Phe1268Cys
XM_011521069.1:c.3773T>G	XP_011519371.1:p.Phe1258Cys
XM_011521070.1:c.3581T>G	XP_011519372.1:p.Phe1194Cys
NM_001350748.1:c.3890T>G	NP_001337677.1:p.Phe1297Cys
NM_001350749.1:c.3803T>G	NP_001337678.1:p.Phe1268Cys
NM_001350750.1:c.3716T>G	NP_001337679.1:p.Phe1239Cys
NM_001350751.1:c.3716T>G	NP_001337680.1:p.Phe1239Cys
NM_052867.3:c.3803T>G	NP_443099.1:p.Phe1268Cys
XM_011521067.2:c.3860T>G	XP_011519369.1:p.Phe1287Cys
XM_011521069.2:c.3773T>G	XP_011519371.1:p.Phe1258Cys
XM_017020536.2:c.3356T>G	XP_016876025.1:p.Phe1119Cys
XM_017020537.1:c.3038T>G	XP_016876026.1:p.Phe1013Cys
XM_024449336.1:c.3947T>G	XP_024305104.1:p.Phe1316Cys
NM_052867.4:c.3803T>G MANE Select	NP_443099.1:p.Phe1268Cys
NM_001350748.2:c.3890T>G	NP_001337677.1:p.Phe1297Cys
NM_001350749.2:c.3803T>G	NP_001337678.1:p.Phe1268Cys
NM_001350750.2:c.3716T>G	NP_001337679.1:p.Phe1239Cys
NM_001350751.2:c.3716T>G	NP_001337680.1:p.Phe1239Cys