Canonical Allele Identifier: CA484554765

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101795554C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101143203C>T , CM000675.2:g.101143203C>T	GRCh38
NC_000013.10:g.101795554C>T , CM000675.1:g.101795554C>T	GRCh37
NC_000013.9:g.100593555C>T	NCBI36
NG_053176.1:g.279004G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1995G>A MANE Select	ENSP00000251127.6:p.Gln665=
ENST00000467264.2:c.187G>A
ENST00000648359.1:c.1995G>A	ENSP00000497465.1:p.Gln665=
ENST00000675150.1:c.1840-18522G>A	ENSP00000502680.1:n.1840-18522G>A
ENST00000675332.1:c.1995G>A	ENSP00000501955.1:p.Gln665=
ENST00000675802.1:c.1995G>A	ENSP00000501818.1:p.Gln665=
ENST00000676315.1:c.1908G>A	ENSP00000501603.1:p.Gln636=
ENST00000251127.10:c.1995G>A	ENSP00000251127.6:p.Gln665=
ENST00000467264.1:n.19G>A
ENST00000497170.5:n.2149G>A
NM_052867.2:c.1995G>A	NP_443099.1:p.Gln665=
XM_011521067.1:c.2052G>A	XP_011519369.1:p.Gln684=
XM_011521068.1:c.1995G>A	XP_011519370.1:p.Gln665=
XM_011521069.1:c.1965G>A	XP_011519371.1:p.Gln655=
XM_011521070.1:c.1897-18522G>A	XP_011519372.1:n.1897-18522G>A
NM_001350748.1:c.1995G>A	NP_001337677.1:p.Gln665=
NM_001350749.1:c.1995G>A	NP_001337678.1:p.Gln665=
NM_001350750.1:c.1908G>A	NP_001337679.1:p.Gln636=
NM_001350751.1:c.1908G>A	NP_001337680.1:p.Gln636=
NM_052867.3:c.1995G>A	NP_443099.1:p.Gln665=
XM_011521067.2:c.2052G>A	XP_011519369.1:p.Gln684=
XM_011521069.2:c.1965G>A	XP_011519371.1:p.Gln655=
XM_017020536.2:c.1548G>A	XP_016876025.1:p.Gln516=
XM_017020537.1:c.1230G>A	XP_016876026.1:p.Gln410=
XM_024449336.1:c.2052G>A	XP_024305104.1:p.Gln684=
NM_052867.4:c.1995G>A MANE Select	NP_443099.1:p.Gln665=
NM_001350748.2:c.1995G>A	NP_001337677.1:p.Gln665=
NM_001350749.2:c.1995G>A	NP_001337678.1:p.Gln665=
NM_001350750.2:c.1908G>A	NP_001337679.1:p.Gln636=
NM_001350751.2:c.1908G>A	NP_001337680.1:p.Gln636=