Canonical Allele Identifier: CA388703585

Gene: NALCN

Linked Data

• COSMIC: COSM945025 ; COSM4867069
• MyVariant Identifiers: chr13:g.101844369C>T (hg19) ; chr13:g.101192018C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101192018C>T , CM000675.2:g.101192018C>T	GRCh38
NC_000013.10:g.101844369C>T , CM000675.1:g.101844369C>T	GRCh37
NC_000013.9:g.100642370C>T	NCBI36
NG_053176.1:g.230189G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1663G>A MANE Select	ENSP00000251127.6:p.Gly555Arg
ENST00000648359.1:c.1663G>A	ENSP00000497465.1:p.Gly555Arg
ENST00000674840.1:n.1761G>A
ENST00000674904.1:n.1743G>A
ENST00000675150.1:c.1663G>A	ENSP00000502680.1:p.Gly555Arg
ENST00000675332.1:c.1663G>A	ENSP00000501955.1:p.Gly555Arg
ENST00000675594.1:c.*1100G>A	ENSP00000502490.1:n.*1100G>A
ENST00000675802.1:c.1663G>A	ENSP00000501818.1:p.Gly555Arg
ENST00000676315.1:c.1576G>A	ENSP00000501603.1:p.Gly526Arg
ENST00000676439.1:n.1837G>A
ENST00000251127.10:c.1663G>A	ENSP00000251127.6:p.Gly555Arg
ENST00000470333.1:n.1759G>A
ENST00000497170.5:n.1817G>A
NM_052867.2:c.1663G>A	NP_443099.1:p.Gly555Arg
XM_011521067.1:c.1720G>A	XP_011519369.1:p.Gly574Arg
XM_011521068.1:c.1663G>A	XP_011519370.1:p.Gly555Arg
XM_011521069.1:c.1633G>A	XP_011519371.1:p.Gly545Arg
XM_011521070.1:c.1720G>A	XP_011519372.1:p.Gly574Arg
NM_001350748.1:c.1663G>A	NP_001337677.1:p.Gly555Arg
NM_001350749.1:c.1663G>A	NP_001337678.1:p.Gly555Arg
NM_001350750.1:c.1576G>A	NP_001337679.1:p.Gly526Arg
NM_001350751.1:c.1576G>A	NP_001337680.1:p.Gly526Arg
NM_052867.3:c.1663G>A	NP_443099.1:p.Gly555Arg
XM_011521067.2:c.1720G>A	XP_011519369.1:p.Gly574Arg
XM_011521069.2:c.1633G>A	XP_011519371.1:p.Gly545Arg
XM_017020536.2:c.1216G>A	XP_016876025.1:p.Gly406Arg
XM_017020537.1:c.898G>A	XP_016876026.1:p.Gly300Arg
XM_024449336.1:c.1720G>A	XP_024305104.1:p.Gly574Arg
NM_052867.4:c.1663G>A MANE Select	NP_443099.1:p.Gly555Arg
NM_001350748.2:c.1663G>A	NP_001337677.1:p.Gly555Arg
NM_001350749.2:c.1663G>A	NP_001337678.1:p.Gly555Arg
NM_001350750.2:c.1576G>A	NP_001337679.1:p.Gly526Arg
NM_001350751.2:c.1576G>A	NP_001337680.1:p.Gly526Arg