Canonical Allele Identifier: CA388650404

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733966G>A (hg19) ; chr13:g.101081615G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081615G>A , CM000675.2:g.101081615G>A	GRCh38
NC_000013.10:g.101733966G>A , CM000675.1:g.101733966G>A	GRCh37
NC_000013.9:g.100531967G>A	NCBI36
NG_053176.1:g.340592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3797C>T MANE Select	ENSP00000251127.6:p.Ala1266Val
ENST00000648359.1:c.3797C>T	ENSP00000497465.1:p.Ala1266Val
ENST00000675150.1:c.3518C>T	ENSP00000502680.1:p.Ala1173Val
ENST00000675332.1:c.3884C>T	ENSP00000501955.1:p.Ala1295Val
ENST00000676315.1:c.3710C>T	ENSP00000501603.1:p.Ala1237Val
ENST00000251127.10:c.3797C>T	ENSP00000251127.6:p.Ala1266Val
NM_052867.2:c.3797C>T	NP_443099.1:p.Ala1266Val
XM_011521067.1:c.3854C>T	XP_011519369.1:p.Ala1285Val
XM_011521068.1:c.3797C>T	XP_011519370.1:p.Ala1266Val
XM_011521069.1:c.3767C>T	XP_011519371.1:p.Ala1256Val
XM_011521070.1:c.3575C>T	XP_011519372.1:p.Ala1192Val
NM_001350748.1:c.3884C>T	NP_001337677.1:p.Ala1295Val
NM_001350749.1:c.3797C>T	NP_001337678.1:p.Ala1266Val
NM_001350750.1:c.3710C>T	NP_001337679.1:p.Ala1237Val
NM_001350751.1:c.3710C>T	NP_001337680.1:p.Ala1237Val
NM_052867.3:c.3797C>T	NP_443099.1:p.Ala1266Val
XM_011521067.2:c.3854C>T	XP_011519369.1:p.Ala1285Val
XM_011521069.2:c.3767C>T	XP_011519371.1:p.Ala1256Val
XM_017020536.2:c.3350C>T	XP_016876025.1:p.Ala1117Val
XM_017020537.1:c.3032C>T	XP_016876026.1:p.Ala1011Val
XM_024449336.1:c.3941C>T	XP_024305104.1:p.Ala1314Val
NM_052867.4:c.3797C>T MANE Select	NP_443099.1:p.Ala1266Val
NM_001350748.2:c.3884C>T	NP_001337677.1:p.Ala1295Val
NM_001350749.2:c.3797C>T	NP_001337678.1:p.Ala1266Val
NM_001350750.2:c.3710C>T	NP_001337679.1:p.Ala1237Val
NM_001350751.2:c.3710C>T	NP_001337680.1:p.Ala1237Val