Canonical Allele Identifier: CA388650510

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733996A>T (hg19) ; chr13:g.101081645A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081645A>T , CM000675.2:g.101081645A>T	GRCh38
NC_000013.10:g.101733996A>T , CM000675.1:g.101733996A>T	GRCh37
NC_000013.9:g.100531997A>T	NCBI36
NG_053176.1:g.340562T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3767T>A MANE Select	ENSP00000251127.6:p.Val1256Asp
ENST00000648359.1:c.3767T>A	ENSP00000497465.1:p.Val1256Asp
ENST00000675150.1:c.3488T>A	ENSP00000502680.1:p.Val1163Asp
ENST00000675332.1:c.3854T>A	ENSP00000501955.1:p.Val1285Asp
ENST00000676315.1:c.3680T>A	ENSP00000501603.1:p.Val1227Asp
ENST00000251127.10:c.3767T>A	ENSP00000251127.6:p.Val1256Asp
NM_052867.2:c.3767T>A	NP_443099.1:p.Val1256Asp
XM_011521067.1:c.3824T>A	XP_011519369.1:p.Val1275Asp
XM_011521068.1:c.3767T>A	XP_011519370.1:p.Val1256Asp
XM_011521069.1:c.3737T>A	XP_011519371.1:p.Val1246Asp
XM_011521070.1:c.3545T>A	XP_011519372.1:p.Val1182Asp
NM_001350748.1:c.3854T>A	NP_001337677.1:p.Val1285Asp
NM_001350749.1:c.3767T>A	NP_001337678.1:p.Val1256Asp
NM_001350750.1:c.3680T>A	NP_001337679.1:p.Val1227Asp
NM_001350751.1:c.3680T>A	NP_001337680.1:p.Val1227Asp
NM_052867.3:c.3767T>A	NP_443099.1:p.Val1256Asp
XM_011521067.2:c.3824T>A	XP_011519369.1:p.Val1275Asp
XM_011521069.2:c.3737T>A	XP_011519371.1:p.Val1246Asp
XM_017020536.2:c.3320T>A	XP_016876025.1:p.Val1107Asp
XM_017020537.1:c.3002T>A	XP_016876026.1:p.Val1001Asp
XM_024449336.1:c.3911T>A	XP_024305104.1:p.Val1304Asp
NM_052867.4:c.3767T>A MANE Select	NP_443099.1:p.Val1256Asp
NM_001350748.2:c.3854T>A	NP_001337677.1:p.Val1285Asp
NM_001350749.2:c.3767T>A	NP_001337678.1:p.Val1256Asp
NM_001350750.2:c.3680T>A	NP_001337679.1:p.Val1227Asp
NM_001350751.2:c.3680T>A	NP_001337680.1:p.Val1227Asp