Canonical Allele Identifier: CA484554803

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101797164A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101144813A>G , CM000675.2:g.101144813A>G	GRCh38
NC_000013.10:g.101797164A>G , CM000675.1:g.101797164A>G	GRCh37
NC_000013.9:g.100595165A>G	NCBI36
NG_053176.1:g.277394T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1923T>C MANE Select	ENSP00000251127.6:p.Pro641=
ENST00000467264.2:c.115T>C
ENST00000648359.1:c.1923T>C	ENSP00000497465.1:p.Pro641=
ENST00000675150.1:c.1840-20132T>C	ENSP00000502680.1:n.1840-20132T>C
ENST00000675332.1:c.1923T>C	ENSP00000501955.1:p.Pro641=
ENST00000675802.1:c.1923T>C	ENSP00000501818.1:p.Pro641=
ENST00000676315.1:c.1836T>C	ENSP00000501603.1:p.Pro612=
ENST00000251127.10:c.1923T>C	ENSP00000251127.6:p.Pro641=
ENST00000497170.5:n.2077T>C
NM_052867.2:c.1923T>C	NP_443099.1:p.Pro641=
XM_011521067.1:c.1980T>C	XP_011519369.1:p.Pro660=
XM_011521068.1:c.1923T>C	XP_011519370.1:p.Pro641=
XM_011521069.1:c.1893T>C	XP_011519371.1:p.Pro631=
XM_011521070.1:c.1897-20132T>C	XP_011519372.1:n.1897-20132T>C
NM_001350748.1:c.1923T>C	NP_001337677.1:p.Pro641=
NM_001350749.1:c.1923T>C	NP_001337678.1:p.Pro641=
NM_001350750.1:c.1836T>C	NP_001337679.1:p.Pro612=
NM_001350751.1:c.1836T>C	NP_001337680.1:p.Pro612=
NM_052867.3:c.1923T>C	NP_443099.1:p.Pro641=
XM_011521067.2:c.1980T>C	XP_011519369.1:p.Pro660=
XM_011521069.2:c.1893T>C	XP_011519371.1:p.Pro631=
XM_017020536.2:c.1476T>C	XP_016876025.1:p.Pro492=
XM_017020537.1:c.1158T>C	XP_016876026.1:p.Pro386=
XM_024449336.1:c.1980T>C	XP_024305104.1:p.Pro660=
NM_052867.4:c.1923T>C MANE Select	NP_443099.1:p.Pro641=
NM_001350748.2:c.1923T>C	NP_001337677.1:p.Pro641=
NM_001350749.2:c.1923T>C	NP_001337678.1:p.Pro641=
NM_001350750.2:c.1836T>C	NP_001337679.1:p.Pro612=
NM_001350751.2:c.1836T>C	NP_001337680.1:p.Pro612=