Canonical Allele Identifier: CA2800371251

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101176402_101176403insCACACCC , CM000675.2:g.101176402_101176403insCACACCC	GRCh38
NC_000013.10:g.101828753_101828754insCACACCC , CM000675.1:g.101828753_101828754insCACACCC	GRCh37
NC_000013.9:g.100626754_100626755insCACACCC	NCBI36
NG_053176.1:g.245804_245805insGGGTGTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1765-29_1765-28insGGGTGTG MANE Select	ENSP00000251127.6:n.1765-29_1765-28insGGGTGTG
ENST00000648359.1:c.1765-29_1765-28insGGGTGTG	ENSP00000497465.1:n.1765-29_1765-28insGGGTGTG
ENST00000674840.1:n.1863-29_1863-28insGGGTGTG
ENST00000675150.1:c.1765-29_1765-28insGGGTGTG	ENSP00000502680.1:n.1765-29_1765-28insGGGTGTG
ENST00000675332.1:c.1765-29_1765-28insGGGTGTG	ENSP00000501955.1:n.1765-29_1765-28insGGGTGTG
ENST00000675802.1:c.1765-29_1765-28insGGGTGTG	ENSP00000501818.1:n.1765-29_1765-28insGGGTGTG
ENST00000675891.1:n.605-29_605-28insGGGTGTG
ENST00000676315.1:c.1678-29_1678-28insGGGTGTG	ENSP00000501603.1:n.1678-29_1678-28insGGGTGTG
ENST00000676439.1:n.1939-29_1939-28insGGGTGTG
ENST00000251127.10:c.1765-29_1765-28insGGGTGTG	ENSP00000251127.6:n.1765-29_1765-28insGGGTGTG
ENST00000497170.5:n.1919-29_1919-28insGGGTGTG
NM_052867.2:c.1765-29_1765-28insGGGTGTG	NP_443099.1:n.1765-29_1765-28insGGGTGTG
XM_011521067.1:c.1822-29_1822-28insGGGTGTG	XP_011519369.1:n.1822-29_1822-28insGGGTGTG
XM_011521068.1:c.1765-29_1765-28insGGGTGTG	XP_011519370.1:n.1765-29_1765-28insGGGTGTG
XM_011521069.1:c.1735-29_1735-28insGGGTGTG	XP_011519371.1:n.1735-29_1735-28insGGGTGTG
XM_011521070.1:c.1822-29_1822-28insGGGTGTG	XP_011519372.1:n.1822-29_1822-28insGGGTGTG
NM_001350748.1:c.1765-29_1765-28insGGGTGTG	NP_001337677.1:n.1765-29_1765-28insGGGTGTG
NM_001350749.1:c.1765-29_1765-28insGGGTGTG	NP_001337678.1:n.1765-29_1765-28insGGGTGTG
NM_001350750.1:c.1678-29_1678-28insGGGTGTG	NP_001337679.1:n.1678-29_1678-28insGGGTGTG
NM_001350751.1:c.1678-29_1678-28insGGGTGTG	NP_001337680.1:n.1678-29_1678-28insGGGTGTG
NM_052867.3:c.1765-29_1765-28insGGGTGTG	NP_443099.1:n.1765-29_1765-28insGGGTGTG
XM_011521067.2:c.1822-29_1822-28insGGGTGTG	XP_011519369.1:n.1822-29_1822-28insGGGTGTG
XM_011521069.2:c.1735-29_1735-28insGGGTGTG	XP_011519371.1:n.1735-29_1735-28insGGGTGTG
XM_017020536.2:c.1318-29_1318-28insGGGTGTG	XP_016876025.1:n.1318-29_1318-28insGGGTGTG
XM_017020537.1:c.1000-29_1000-28insGGGTGTG	XP_016876026.1:n.1000-29_1000-28insGGGTGTG
XM_024449336.1:c.1822-29_1822-28insGGGTGTG	XP_024305104.1:n.1822-29_1822-28insGGGTGTG
NM_052867.4:c.1765-29_1765-28insGGGTGTG MANE Select	NP_443099.1:n.1765-29_1765-28insGGGTGTG
NM_001350748.2:c.1765-29_1765-28insGGGTGTG	NP_001337677.1:n.1765-29_1765-28insGGGTGTG
NM_001350749.2:c.1765-29_1765-28insGGGTGTG	NP_001337678.1:n.1765-29_1765-28insGGGTGTG
NM_001350750.2:c.1678-29_1678-28insGGGTGTG	NP_001337679.1:n.1678-29_1678-28insGGGTGTG
NM_001350751.2:c.1678-29_1678-28insGGGTGTG	NP_001337680.1:n.1678-29_1678-28insGGGTGTG