Canonical Allele Identifier: CA484763927

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101944668C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292317C>A , CM000675.2:g.101292317C>A	GRCh38
NC_000013.10:g.101944668C>A , CM000675.1:g.101944668C>A	GRCh37
NC_000013.9:g.100742669C>A	NCBI36
NG_053176.1:g.129890G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.849G>T MANE Select	ENSP00000251127.6:p.Val283=
ENST00000648359.1:c.849G>T	ENSP00000497465.1:p.Val283=
ENST00000674840.1:n.947G>T
ENST00000674904.1:n.929G>T
ENST00000675075.1:n.451G>T
ENST00000675150.1:c.849G>T	ENSP00000502680.1:p.Val283=
ENST00000675332.1:c.849G>T	ENSP00000501955.1:p.Val283=
ENST00000675415.1:n.1032G>T
ENST00000675594.1:c.*286G>T	ENSP00000502490.1:n.*286G>T
ENST00000675802.1:c.849G>T	ENSP00000501818.1:p.Val283=
ENST00000676315.1:c.849G>T	ENSP00000501603.1:p.Val283=
ENST00000676439.1:n.1023G>T
ENST00000251127.10:c.849G>T	ENSP00000251127.6:p.Val283=
ENST00000470333.1:n.945G>T
ENST00000497170.5:n.1003G>T
NM_052867.2:c.849G>T	NP_443099.1:p.Val283=
XM_011521067.1:c.906G>T	XP_011519369.1:p.Val302=
XM_011521068.1:c.849G>T	XP_011519370.1:p.Val283=
XM_011521069.1:c.906G>T	XP_011519371.1:p.Val302=
XM_011521070.1:c.906G>T	XP_011519372.1:p.Val302=
NM_001350748.1:c.849G>T	NP_001337677.1:p.Val283=
NM_001350749.1:c.849G>T	NP_001337678.1:p.Val283=
NM_001350750.1:c.849G>T	NP_001337679.1:p.Val283=
NM_001350751.1:c.849G>T	NP_001337680.1:p.Val283=
NM_052867.3:c.849G>T	NP_443099.1:p.Val283=
XM_011521067.2:c.906G>T	XP_011519369.1:p.Val302=
XM_011521069.2:c.906G>T	XP_011519371.1:p.Val302=
XM_017020536.2:c.402G>T	XP_016876025.1:p.Val134=
XM_017020537.1:c.84G>T	XP_016876026.1:p.Val28=
XM_024449336.1:c.906G>T	XP_024305104.1:p.Val302=
NM_052867.4:c.849G>T MANE Select	NP_443099.1:p.Val283=
NM_001350748.2:c.849G>T	NP_001337677.1:p.Val283=
NM_001350749.2:c.849G>T	NP_001337678.1:p.Val283=
NM_001350750.2:c.849G>T	NP_001337679.1:p.Val283=
NM_001350751.2:c.849G>T	NP_001337680.1:p.Val283=