Canonical Allele Identifier: CA484769755

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.102029170T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101376819T>A , CM000675.2:g.101376819T>A	GRCh38
NC_000013.10:g.102029170T>A , CM000675.1:g.102029170T>A	GRCh37
NC_000013.9:g.100827171T>A	NCBI36
NG_053176.1:g.45388A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.525A>T MANE Select	ENSP00000251127.6:p.Gly175=
ENST00000376200.6:c.525A>T	ENSP00000365373.5:p.Gly175=
ENST00000648359.1:c.525A>T	ENSP00000497465.1:p.Gly175=
ENST00000674840.1:n.623A>T
ENST00000674904.1:n.605A>T
ENST00000675150.1:c.525A>T	ENSP00000502680.1:p.Gly175=
ENST00000675332.1:c.525A>T	ENSP00000501955.1:p.Gly175=
ENST00000675415.1:n.708A>T
ENST00000675594.1:c.525A>T	ENSP00000502490.1:p.Gly175=
ENST00000675802.1:c.525A>T	ENSP00000501818.1:p.Gly175=
ENST00000676315.1:c.525A>T	ENSP00000501603.1:p.Gly175=
ENST00000676357.1:n.745A>T
ENST00000676439.1:n.699A>T
ENST00000251127.10:c.525A>T	ENSP00000251127.6:p.Gly175=
ENST00000376200.5:c.525A>T	ENSP00000365373.5:p.Gly175=
ENST00000470333.1:n.621A>T
ENST00000497170.5:n.714A>T
NM_052867.2:c.525A>T	NP_443099.1:p.Gly175=
XM_011521067.1:c.582A>T	XP_011519369.1:p.Gly194=
XM_011521068.1:c.525A>T	XP_011519370.1:p.Gly175=
XM_011521069.1:c.582A>T	XP_011519371.1:p.Gly194=
XM_011521070.1:c.582A>T	XP_011519372.1:p.Gly194=
NM_001350748.1:c.525A>T	NP_001337677.1:p.Gly175=
NM_001350749.1:c.525A>T	NP_001337678.1:p.Gly175=
NM_001350750.1:c.525A>T	NP_001337679.1:p.Gly175=
NM_001350751.1:c.525A>T	NP_001337680.1:p.Gly175=
NM_052867.3:c.525A>T	NP_443099.1:p.Gly175=
XM_011521067.2:c.582A>T	XP_011519369.1:p.Gly194=
XM_011521069.2:c.582A>T	XP_011519371.1:p.Gly194=
XM_024449336.1:c.582A>T	XP_024305104.1:p.Gly194=
NM_052867.4:c.525A>T MANE Select	NP_443099.1:p.Gly175=
NM_001350748.2:c.525A>T	NP_001337677.1:p.Gly175=
NM_001350749.2:c.525A>T	NP_001337678.1:p.Gly175=
NM_001350750.2:c.525A>T	NP_001337679.1:p.Gly175=
NM_001350751.2:c.525A>T	NP_001337680.1:p.Gly175=