Canonical Allele Identifier: CA484554762

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101795548A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101143197A>G , CM000675.2:g.101143197A>G	GRCh38
NC_000013.10:g.101795548A>G , CM000675.1:g.101795548A>G	GRCh37
NC_000013.9:g.100593549A>G	NCBI36
NG_053176.1:g.279010T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.2001T>C MANE Select	ENSP00000251127.6:p.Ile667=
ENST00000467264.2:c.193T>C
ENST00000648359.1:c.2001T>C	ENSP00000497465.1:p.Ile667=
ENST00000675150.1:c.1840-18516T>C	ENSP00000502680.1:n.1840-18516T>C
ENST00000675332.1:c.2001T>C	ENSP00000501955.1:p.Ile667=
ENST00000675802.1:c.2001T>C	ENSP00000501818.1:p.Ile667=
ENST00000676315.1:c.1914T>C	ENSP00000501603.1:p.Ile638=
ENST00000251127.10:c.2001T>C	ENSP00000251127.6:p.Ile667=
ENST00000467264.1:n.25T>C
ENST00000497170.5:n.2155T>C
NM_052867.2:c.2001T>C	NP_443099.1:p.Ile667=
XM_011521067.1:c.2058T>C	XP_011519369.1:p.Ile686=
XM_011521068.1:c.2001T>C	XP_011519370.1:p.Ile667=
XM_011521069.1:c.1971T>C	XP_011519371.1:p.Ile657=
XM_011521070.1:c.1897-18516T>C	XP_011519372.1:n.1897-18516T>C
NM_001350748.1:c.2001T>C	NP_001337677.1:p.Ile667=
NM_001350749.1:c.2001T>C	NP_001337678.1:p.Ile667=
NM_001350750.1:c.1914T>C	NP_001337679.1:p.Ile638=
NM_001350751.1:c.1914T>C	NP_001337680.1:p.Ile638=
NM_052867.3:c.2001T>C	NP_443099.1:p.Ile667=
XM_011521067.2:c.2058T>C	XP_011519369.1:p.Ile686=
XM_011521069.2:c.1971T>C	XP_011519371.1:p.Ile657=
XM_017020536.2:c.1554T>C	XP_016876025.1:p.Ile518=
XM_017020537.1:c.1236T>C	XP_016876026.1:p.Ile412=
XM_024449336.1:c.2058T>C	XP_024305104.1:p.Ile686=
NM_052867.4:c.2001T>C MANE Select	NP_443099.1:p.Ile667=
NM_001350748.2:c.2001T>C	NP_001337677.1:p.Ile667=
NM_001350749.2:c.2001T>C	NP_001337678.1:p.Ile667=
NM_001350750.2:c.1914T>C	NP_001337679.1:p.Ile638=
NM_001350751.2:c.1914T>C	NP_001337680.1:p.Ile638=