Canonical Allele Identifier: CA2800372867

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292165_101292166insCACCCAACAC , CM000675.2:g.101292165_101292166insCACCCAACAC	GRCh38
NC_000013.10:g.101944516_101944517insCACCCAACAC , CM000675.1:g.101944516_101944517insCACCCAACAC	GRCh37
NC_000013.9:g.100742517_100742518insCACCCAACAC	NCBI36
NG_053176.1:g.130041_130042insGTGTTGGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.942+58_942+59insGTGTTGGGTG MANE Select	ENSP00000251127.6:n.942+58_942+59insGTGTTGGGTG
ENST00000648359.1:c.942+58_942+59insGTGTTGGGTG	ENSP00000497465.1:n.942+58_942+59insGTGTTGGGTG
ENST00000674840.1:n.1040+58_1040+59insGTGTTGGGTG
ENST00000674904.1:n.1022+58_1022+59insGTGTTGGGTG
ENST00000675075.1:n.544+58_544+59insGTGTTGGGTG
ENST00000675150.1:c.942+58_942+59insGTGTTGGGTG	ENSP00000502680.1:n.942+58_942+59insGTGTTGGGTG
ENST00000675332.1:c.942+58_942+59insGTGTTGGGTG	ENSP00000501955.1:n.942+58_942+59insGTGTTGGGTG
ENST00000675415.1:n.1125+58_1125+59insGTGTTGGGTG
ENST00000675594.1:c.*379+58_*379+59insGTGTTGGGTG	ENSP00000502490.1:n.*379+58_*379+59insGTGTTGGGTG
ENST00000675802.1:c.942+58_942+59insGTGTTGGGTG	ENSP00000501818.1:n.942+58_942+59insGTGTTGGGTG
ENST00000676315.1:c.942+58_942+59insGTGTTGGGTG	ENSP00000501603.1:n.942+58_942+59insGTGTTGGGTG
ENST00000676439.1:n.1116+58_1116+59insGTGTTGGGTG
ENST00000251127.10:c.942+58_942+59insGTGTTGGGTG	ENSP00000251127.6:n.942+58_942+59insGTGTTGGGTG
ENST00000470333.1:n.1038+58_1038+59insGTGTTGGGTG
ENST00000497170.5:n.1096+58_1096+59insGTGTTGGGTG
NM_052867.2:c.942+58_942+59insGTGTTGGGTG	NP_443099.1:n.942+58_942+59insGTGTTGGGTG
XM_011521067.1:c.999+58_999+59insGTGTTGGGTG	XP_011519369.1:n.999+58_999+59insGTGTTGGGTG
XM_011521068.1:c.942+58_942+59insGTGTTGGGTG	XP_011519370.1:n.942+58_942+59insGTGTTGGGTG
XM_011521069.1:c.999+58_999+59insGTGTTGGGTG	XP_011519371.1:n.999+58_999+59insGTGTTGGGTG
XM_011521070.1:c.999+58_999+59insGTGTTGGGTG	XP_011519372.1:n.999+58_999+59insGTGTTGGGTG
NM_001350748.1:c.942+58_942+59insGTGTTGGGTG	NP_001337677.1:n.942+58_942+59insGTGTTGGGTG
NM_001350749.1:c.942+58_942+59insGTGTTGGGTG	NP_001337678.1:n.942+58_942+59insGTGTTGGGTG
NM_001350750.1:c.942+58_942+59insGTGTTGGGTG	NP_001337679.1:n.942+58_942+59insGTGTTGGGTG
NM_001350751.1:c.942+58_942+59insGTGTTGGGTG	NP_001337680.1:n.942+58_942+59insGTGTTGGGTG
NM_052867.3:c.942+58_942+59insGTGTTGGGTG	NP_443099.1:n.942+58_942+59insGTGTTGGGTG
XM_011521067.2:c.999+58_999+59insGTGTTGGGTG	XP_011519369.1:n.999+58_999+59insGTGTTGGGTG
XM_011521069.2:c.999+58_999+59insGTGTTGGGTG	XP_011519371.1:n.999+58_999+59insGTGTTGGGTG
XM_017020536.2:c.495+58_495+59insGTGTTGGGTG	XP_016876025.1:n.495+58_495+59insGTGTTGGGTG
XM_017020537.1:c.177+58_177+59insGTGTTGGGTG	XP_016876026.1:n.177+58_177+59insGTGTTGGGTG
XM_024449336.1:c.999+58_999+59insGTGTTGGGTG	XP_024305104.1:n.999+58_999+59insGTGTTGGGTG
NM_052867.4:c.942+58_942+59insGTGTTGGGTG MANE Select	NP_443099.1:n.942+58_942+59insGTGTTGGGTG
NM_001350748.2:c.942+58_942+59insGTGTTGGGTG	NP_001337677.1:n.942+58_942+59insGTGTTGGGTG
NM_001350749.2:c.942+58_942+59insGTGTTGGGTG	NP_001337678.1:n.942+58_942+59insGTGTTGGGTG
NM_001350750.2:c.942+58_942+59insGTGTTGGGTG	NP_001337679.1:n.942+58_942+59insGTGTTGGGTG
NM_001350751.2:c.942+58_942+59insGTGTTGGGTG	NP_001337680.1:n.942+58_942+59insGTGTTGGGTG