Canonical Allele Identifier: CA388671576

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101795558T>A (hg19) ; chr13:g.101143207T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101143207T>A , CM000675.2:g.101143207T>A	GRCh38
NC_000013.10:g.101795558T>A , CM000675.1:g.101795558T>A	GRCh37
NC_000013.9:g.100593559T>A	NCBI36
NG_053176.1:g.279000A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1991A>T MANE Select	ENSP00000251127.6:p.Lys664Met
ENST00000467264.2:c.183A>T
ENST00000648359.1:c.1991A>T	ENSP00000497465.1:p.Lys664Met
ENST00000675150.1:c.1840-18526A>T	ENSP00000502680.1:n.1840-18526A>T
ENST00000675332.1:c.1991A>T	ENSP00000501955.1:p.Lys664Met
ENST00000675802.1:c.1991A>T	ENSP00000501818.1:p.Lys664Met
ENST00000676315.1:c.1904A>T	ENSP00000501603.1:p.Lys635Met
ENST00000251127.10:c.1991A>T	ENSP00000251127.6:p.Lys664Met
ENST00000467264.1:n.15A>T
ENST00000497170.5:n.2145A>T
NM_052867.2:c.1991A>T	NP_443099.1:p.Lys664Met
XM_011521067.1:c.2048A>T	XP_011519369.1:p.Lys683Met
XM_011521068.1:c.1991A>T	XP_011519370.1:p.Lys664Met
XM_011521069.1:c.1961A>T	XP_011519371.1:p.Lys654Met
XM_011521070.1:c.1897-18526A>T	XP_011519372.1:n.1897-18526A>T
NM_001350748.1:c.1991A>T	NP_001337677.1:p.Lys664Met
NM_001350749.1:c.1991A>T	NP_001337678.1:p.Lys664Met
NM_001350750.1:c.1904A>T	NP_001337679.1:p.Lys635Met
NM_001350751.1:c.1904A>T	NP_001337680.1:p.Lys635Met
NM_052867.3:c.1991A>T	NP_443099.1:p.Lys664Met
XM_011521067.2:c.2048A>T	XP_011519369.1:p.Lys683Met
XM_011521069.2:c.1961A>T	XP_011519371.1:p.Lys654Met
XM_017020536.2:c.1544A>T	XP_016876025.1:p.Lys515Met
XM_017020537.1:c.1226A>T	XP_016876026.1:p.Lys409Met
XM_024449336.1:c.2048A>T	XP_024305104.1:p.Lys683Met
NM_052867.4:c.1991A>T MANE Select	NP_443099.1:p.Lys664Met
NM_001350748.2:c.1991A>T	NP_001337677.1:p.Lys664Met
NM_001350749.2:c.1991A>T	NP_001337678.1:p.Lys664Met
NM_001350750.2:c.1904A>T	NP_001337679.1:p.Lys635Met
NM_001350751.2:c.1904A>T	NP_001337680.1:p.Lys635Met