Canonical Allele Identifier: CA388650289

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733932A>T (hg19) ; chr13:g.101081581A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081581A>T , CM000675.2:g.101081581A>T	GRCh38
NC_000013.10:g.101733932A>T , CM000675.1:g.101733932A>T	GRCh37
NC_000013.9:g.100531933A>T	NCBI36
NG_053176.1:g.340626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3831T>A MANE Select	ENSP00000251127.6:p.Asp1277Glu
ENST00000648359.1:c.3831T>A	ENSP00000497465.1:p.Asp1277Glu
ENST00000675150.1:c.3552T>A	ENSP00000502680.1:p.Asp1184Glu
ENST00000675332.1:c.3918T>A	ENSP00000501955.1:p.Asp1306Glu
ENST00000676315.1:c.3744T>A	ENSP00000501603.1:p.Asp1248Glu
ENST00000251127.10:c.3831T>A	ENSP00000251127.6:p.Asp1277Glu
NM_052867.2:c.3831T>A	NP_443099.1:p.Asp1277Glu
XM_011521067.1:c.3888T>A	XP_011519369.1:p.Asp1296Glu
XM_011521068.1:c.3831T>A	XP_011519370.1:p.Asp1277Glu
XM_011521069.1:c.3801T>A	XP_011519371.1:p.Asp1267Glu
XM_011521070.1:c.3609T>A	XP_011519372.1:p.Asp1203Glu
NM_001350748.1:c.3918T>A	NP_001337677.1:p.Asp1306Glu
NM_001350749.1:c.3831T>A	NP_001337678.1:p.Asp1277Glu
NM_001350750.1:c.3744T>A	NP_001337679.1:p.Asp1248Glu
NM_001350751.1:c.3744T>A	NP_001337680.1:p.Asp1248Glu
NM_052867.3:c.3831T>A	NP_443099.1:p.Asp1277Glu
XM_011521067.2:c.3888T>A	XP_011519369.1:p.Asp1296Glu
XM_011521069.2:c.3801T>A	XP_011519371.1:p.Asp1267Glu
XM_017020536.2:c.3384T>A	XP_016876025.1:p.Asp1128Glu
XM_017020537.1:c.3066T>A	XP_016876026.1:p.Asp1022Glu
XM_024449336.1:c.3975T>A	XP_024305104.1:p.Asp1325Glu
NM_052867.4:c.3831T>A MANE Select	NP_443099.1:p.Asp1277Glu
NM_001350748.2:c.3918T>A	NP_001337677.1:p.Asp1306Glu
NM_001350749.2:c.3831T>A	NP_001337678.1:p.Asp1277Glu
NM_001350750.2:c.3744T>A	NP_001337679.1:p.Asp1248Glu
NM_001350751.2:c.3744T>A	NP_001337680.1:p.Asp1248Glu