Canonical Allele Identifier: CA484552291

Gene: NALCN

Linked Data

• gnomAD v4: 13-101081617-A-T
• MyVariant Identifiers: chr13:g.101733968A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081617A>T , CM000675.2:g.101081617A>T	GRCh38
NC_000013.10:g.101733968A>T , CM000675.1:g.101733968A>T	GRCh37
NC_000013.9:g.100531969A>T	NCBI36
NG_053176.1:g.340590T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3795T>A MANE Select	ENSP00000251127.6:p.Pro1265=
ENST00000648359.1:c.3795T>A	ENSP00000497465.1:p.Pro1265=
ENST00000675150.1:c.3516T>A	ENSP00000502680.1:p.Pro1172=
ENST00000675332.1:c.3882T>A	ENSP00000501955.1:p.Pro1294=
ENST00000676315.1:c.3708T>A	ENSP00000501603.1:p.Pro1236=
ENST00000251127.10:c.3795T>A	ENSP00000251127.6:p.Pro1265=
NM_052867.2:c.3795T>A	NP_443099.1:p.Pro1265=
XM_011521067.1:c.3852T>A	XP_011519369.1:p.Pro1284=
XM_011521068.1:c.3795T>A	XP_011519370.1:p.Pro1265=
XM_011521069.1:c.3765T>A	XP_011519371.1:p.Pro1255=
XM_011521070.1:c.3573T>A	XP_011519372.1:p.Pro1191=
NM_001350748.1:c.3882T>A	NP_001337677.1:p.Pro1294=
NM_001350749.1:c.3795T>A	NP_001337678.1:p.Pro1265=
NM_001350750.1:c.3708T>A	NP_001337679.1:p.Pro1236=
NM_001350751.1:c.3708T>A	NP_001337680.1:p.Pro1236=
NM_052867.3:c.3795T>A	NP_443099.1:p.Pro1265=
XM_011521067.2:c.3852T>A	XP_011519369.1:p.Pro1284=
XM_011521069.2:c.3765T>A	XP_011519371.1:p.Pro1255=
XM_017020536.2:c.3348T>A	XP_016876025.1:p.Pro1116=
XM_017020537.1:c.3030T>A	XP_016876026.1:p.Pro1010=
XM_024449336.1:c.3939T>A	XP_024305104.1:p.Pro1313=
NM_052867.4:c.3795T>A MANE Select	NP_443099.1:p.Pro1265=
NM_001350748.2:c.3882T>A	NP_001337677.1:p.Pro1294=
NM_001350749.2:c.3795T>A	NP_001337678.1:p.Pro1265=
NM_001350750.2:c.3708T>A	NP_001337679.1:p.Pro1236=
NM_001350751.2:c.3708T>A	NP_001337680.1:p.Pro1236=