Canonical Allele Identifier: CA484551817

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733893A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081542A>T , CM000675.2:g.101081542A>T	GRCh38
NC_000013.10:g.101733893A>T , CM000675.1:g.101733893A>T	GRCh37
NC_000013.9:g.100531894A>T	NCBI36
NG_053176.1:g.340665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3870T>A MANE Select	ENSP00000251127.6:p.Leu1290=
ENST00000648359.1:c.3870T>A	ENSP00000497465.1:p.Leu1290=
ENST00000675150.1:c.3591T>A	ENSP00000502680.1:p.Leu1197=
ENST00000675332.1:c.3957T>A	ENSP00000501955.1:p.Leu1319=
ENST00000676315.1:c.3783T>A	ENSP00000501603.1:p.Leu1261=
ENST00000251127.10:c.3870T>A	ENSP00000251127.6:p.Leu1290=
NM_052867.2:c.3870T>A	NP_443099.1:p.Leu1290=
XM_011521067.1:c.3927T>A	XP_011519369.1:p.Leu1309=
XM_011521068.1:c.3870T>A	XP_011519370.1:p.Leu1290=
XM_011521069.1:c.3840T>A	XP_011519371.1:p.Leu1280=
XM_011521070.1:c.3648T>A	XP_011519372.1:p.Leu1216=
NM_001350748.1:c.3957T>A	NP_001337677.1:p.Leu1319=
NM_001350749.1:c.3870T>A	NP_001337678.1:p.Leu1290=
NM_001350750.1:c.3783T>A	NP_001337679.1:p.Leu1261=
NM_001350751.1:c.3783T>A	NP_001337680.1:p.Leu1261=
NM_052867.3:c.3870T>A	NP_443099.1:p.Leu1290=
XM_011521067.2:c.3927T>A	XP_011519369.1:p.Leu1309=
XM_011521069.2:c.3840T>A	XP_011519371.1:p.Leu1280=
XM_017020536.2:c.3423T>A	XP_016876025.1:p.Leu1141=
XM_017020537.1:c.3105T>A	XP_016876026.1:p.Leu1035=
XM_024449336.1:c.4014T>A	XP_024305104.1:p.Leu1338=
NM_052867.4:c.3870T>A MANE Select	NP_443099.1:p.Leu1290=
NM_001350748.2:c.3957T>A	NP_001337677.1:p.Leu1319=
NM_001350749.2:c.3870T>A	NP_001337678.1:p.Leu1290=
NM_001350750.2:c.3783T>A	NP_001337679.1:p.Leu1261=
NM_001350751.2:c.3783T>A	NP_001337680.1:p.Leu1261=