Canonical Allele Identifier: CA484553416

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101736114G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101083763G>A , CM000675.2:g.101083763G>A	GRCh38
NC_000013.10:g.101736114G>A , CM000675.1:g.101736114G>A	GRCh37
NC_000013.9:g.100534115G>A	NCBI36
NG_053176.1:g.338444C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3531C>T MANE Select	ENSP00000251127.6:p.Asp1177=
ENST00000648359.1:c.3531C>T	ENSP00000497465.1:p.Asp1177=
ENST00000675150.1:c.3252C>T	ENSP00000502680.1:p.Asp1084=
ENST00000675332.1:c.3618C>T	ENSP00000501955.1:p.Asp1206=
ENST00000676315.1:c.3444C>T	ENSP00000501603.1:p.Asp1148=
ENST00000251127.10:c.3531C>T	ENSP00000251127.6:p.Asp1177=
NM_052867.2:c.3531C>T	NP_443099.1:p.Asp1177=
XM_011521067.1:c.3588C>T	XP_011519369.1:p.Asp1196=
XM_011521068.1:c.3531C>T	XP_011519370.1:p.Asp1177=
XM_011521069.1:c.3501C>T	XP_011519371.1:p.Asp1167=
XM_011521070.1:c.3309C>T	XP_011519372.1:p.Asp1103=
NM_001350748.1:c.3618C>T	NP_001337677.1:p.Asp1206=
NM_001350749.1:c.3531C>T	NP_001337678.1:p.Asp1177=
NM_001350750.1:c.3444C>T	NP_001337679.1:p.Asp1148=
NM_001350751.1:c.3444C>T	NP_001337680.1:p.Asp1148=
NM_052867.3:c.3531C>T	NP_443099.1:p.Asp1177=
XM_011521067.2:c.3588C>T	XP_011519369.1:p.Asp1196=
XM_011521069.2:c.3501C>T	XP_011519371.1:p.Asp1167=
XM_017020536.2:c.3084C>T	XP_016876025.1:p.Asp1028=
XM_017020537.1:c.2766C>T	XP_016876026.1:p.Asp922=
XM_024449336.1:c.3675C>T	XP_024305104.1:p.Asp1225=
NM_052867.4:c.3531C>T MANE Select	NP_443099.1:p.Asp1177=
NM_001350748.2:c.3618C>T	NP_001337677.1:p.Asp1206=
NM_001350749.2:c.3531C>T	NP_001337678.1:p.Asp1177=
NM_001350750.2:c.3444C>T	NP_001337679.1:p.Asp1148=
NM_001350751.2:c.3444C>T	NP_001337680.1:p.Asp1148=