Canonical Allele Identifier: CA2114432021

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101176272_101176273delinsTA , CM000675.2:g.101176272_101176273delinsTA	GRCh38
NC_000013.10:g.101828623_101828624delinsTA , CM000675.1:g.101828623_101828624delinsTA	GRCh37
NC_000013.9:g.100626624_100626625delinsTA	NCBI36
NG_053176.1:g.245934_245935delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1839+27_1839+28delinsTA MANE Select	ENSP00000251127.6:n.1839+27_1839+28delins...
ENST00000467264.2:c.31+27_31+28delinsTA
ENST00000648359.1:c.1839+27_1839+28delinsTA	ENSP00000497465.1:n.1839+27_1839+28delins...
ENST00000674840.1:n.1937+27_1937+28delinsTA
ENST00000675150.1:c.1839+27_1839+28delinsTA	ENSP00000502680.1:n.1839+27_1839+28delins...
ENST00000675332.1:c.1839+27_1839+28delinsTA	ENSP00000501955.1:n.1839+27_1839+28delins...
ENST00000675802.1:c.1839+27_1839+28delinsTA	ENSP00000501818.1:n.1839+27_1839+28delins...
ENST00000676315.1:c.1752+27_1752+28delinsTA	ENSP00000501603.1:n.1752+27_1752+28delins...
ENST00000676439.1:n.2013+27_2013+28delinsTA
ENST00000251127.10:c.1839+27_1839+28delinsTA	ENSP00000251127.6:n.1839+27_1839+28delins...
ENST00000497170.5:n.1993+27_1993+28delinsTA
NM_052867.2:c.1839+27_1839+28delinsTA	NP_443099.1:n.1839+27_1839+28delinsTA
XM_011521067.1:c.1896+27_1896+28delinsTA	XP_011519369.1:n.1896+27_1896+28delinsTA
XM_011521068.1:c.1839+27_1839+28delinsTA	XP_011519370.1:n.1839+27_1839+28delinsTA
XM_011521069.1:c.1809+27_1809+28delinsTA	XP_011519371.1:n.1809+27_1809+28delinsTA
XM_011521070.1:c.1896+27_1896+28delinsTA	XP_011519372.1:n.1896+27_1896+28delinsTA
NM_001350748.1:c.1839+27_1839+28delinsTA	NP_001337677.1:n.1839+27_1839+28delinsTA
NM_001350749.1:c.1839+27_1839+28delinsTA	NP_001337678.1:n.1839+27_1839+28delinsTA
NM_001350750.1:c.1752+27_1752+28delinsTA	NP_001337679.1:n.1752+27_1752+28delinsTA
NM_001350751.1:c.1752+27_1752+28delinsTA	NP_001337680.1:n.1752+27_1752+28delinsTA
NM_052867.3:c.1839+27_1839+28delinsTA	NP_443099.1:n.1839+27_1839+28delinsTA
XM_011521067.2:c.1896+27_1896+28delinsTA	XP_011519369.1:n.1896+27_1896+28delinsTA
XM_011521069.2:c.1809+27_1809+28delinsTA	XP_011519371.1:n.1809+27_1809+28delinsTA
XM_017020536.2:c.1392+27_1392+28delinsTA	XP_016876025.1:n.1392+27_1392+28delinsTA
XM_017020537.1:c.1074+27_1074+28delinsTA	XP_016876026.1:n.1074+27_1074+28delinsTA
XM_024449336.1:c.1896+27_1896+28delinsTA	XP_024305104.1:n.1896+27_1896+28delinsTA
NM_052867.4:c.1839+27_1839+28delinsTA MANE Select	NP_443099.1:n.1839+27_1839+28delinsTA
NM_001350748.2:c.1839+27_1839+28delinsTA	NP_001337677.1:n.1839+27_1839+28delinsTA
NM_001350749.2:c.1839+27_1839+28delinsTA	NP_001337678.1:n.1839+27_1839+28delinsTA
NM_001350750.2:c.1752+27_1752+28delinsTA	NP_001337679.1:n.1752+27_1752+28delinsTA
NM_001350751.2:c.1752+27_1752+28delinsTA	NP_001337680.1:n.1752+27_1752+28delinsTA