Canonical Allele Identifier: CA388705537

Gene: NALCN

Linked Data

• dbSNP Id: rs2139420356
• MyVariant Identifiers: chr13:g.102029180C>A (hg19) ; chr13:g.101376829C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101376829C>A , CM000675.2:g.101376829C>A	GRCh38
NC_000013.10:g.102029180C>A , CM000675.1:g.102029180C>A	GRCh37
NC_000013.9:g.100827181C>A	NCBI36
NG_053176.1:g.45378G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.516-1G>T MANE Select	ENSP00000251127.6:n.516-1G>T
ENST00000376200.6:c.516-1G>T	ENSP00000365373.5:n.516-1G>T
ENST00000648359.1:c.516-1G>T	ENSP00000497465.1:n.516-1G>T
ENST00000674840.1:n.614-1G>T
ENST00000674904.1:n.596-1G>T
ENST00000675150.1:c.516-1G>T	ENSP00000502680.1:n.516-1G>T
ENST00000675332.1:c.516-1G>T	ENSP00000501955.1:n.516-1G>T
ENST00000675415.1:n.699-1G>T
ENST00000675594.1:c.516-1G>T	ENSP00000502490.1:n.516-1G>T
ENST00000675802.1:c.516-1G>T	ENSP00000501818.1:n.516-1G>T
ENST00000676315.1:c.516-1G>T	ENSP00000501603.1:n.516-1G>T
ENST00000676357.1:n.736-1G>T
ENST00000676439.1:n.690-1G>T
ENST00000251127.10:c.516-1G>T	ENSP00000251127.6:n.516-1G>T
ENST00000376200.5:c.516-1G>T	ENSP00000365373.5:n.516-1G>T
ENST00000470333.1:n.612-1G>T
ENST00000497170.5:n.705-1G>T
NM_052867.2:c.516-1G>T	NP_443099.1:n.516-1G>T
XM_011521067.1:c.573-1G>T	XP_011519369.1:n.573-1G>T
XM_011521068.1:c.516-1G>T	XP_011519370.1:n.516-1G>T
XM_011521069.1:c.573-1G>T	XP_011519371.1:n.573-1G>T
XM_011521070.1:c.573-1G>T	XP_011519372.1:n.573-1G>T
NM_001350748.1:c.516-1G>T	NP_001337677.1:n.516-1G>T
NM_001350749.1:c.516-1G>T	NP_001337678.1:n.516-1G>T
NM_001350750.1:c.516-1G>T	NP_001337679.1:n.516-1G>T
NM_001350751.1:c.516-1G>T	NP_001337680.1:n.516-1G>T
NM_052867.3:c.516-1G>T	NP_443099.1:n.516-1G>T
XM_011521067.2:c.573-1G>T	XP_011519369.1:n.573-1G>T
XM_011521069.2:c.573-1G>T	XP_011519371.1:n.573-1G>T
XM_024449336.1:c.573-1G>T	XP_024305104.1:n.573-1G>T
NM_052867.4:c.516-1G>T MANE Select	NP_443099.1:n.516-1G>T
NM_001350748.2:c.516-1G>T	NP_001337677.1:n.516-1G>T
NM_001350749.2:c.516-1G>T	NP_001337678.1:n.516-1G>T
NM_001350750.2:c.516-1G>T	NP_001337679.1:n.516-1G>T
NM_001350751.2:c.516-1G>T	NP_001337680.1:n.516-1G>T