Canonical Allele Identifier: CA2526176040

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292204_101292205insAATGT , CM000675.2:g.101292204_101292205insAATGT	GRCh38
NC_000013.10:g.101944555_101944556insAATGT , CM000675.1:g.101944555_101944556insAATGT	GRCh37
NC_000013.9:g.100742556_100742557insAATGT	NCBI36
NG_053176.1:g.130002_130003insACATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.942+19_942+20insACATT MANE Select	ENSP00000251127.6:n.942+19_942+20insACATT
ENST00000648359.1:c.942+19_942+20insACATT	ENSP00000497465.1:n.942+19_942+20insACATT
ENST00000674840.1:n.1040+19_1040+20insACATT
ENST00000674904.1:n.1022+19_1022+20insACATT
ENST00000675075.1:n.544+19_544+20insACATT
ENST00000675150.1:c.942+19_942+20insACATT	ENSP00000502680.1:n.942+19_942+20insACATT
ENST00000675332.1:c.942+19_942+20insACATT	ENSP00000501955.1:n.942+19_942+20insACATT
ENST00000675415.1:n.1125+19_1125+20insACATT
ENST00000675594.1:c.*379+19_*379+20insACATT	ENSP00000502490.1:n.*379+19_*379+20insACATT
ENST00000675802.1:c.942+19_942+20insACATT	ENSP00000501818.1:n.942+19_942+20insACATT
ENST00000676315.1:c.942+19_942+20insACATT	ENSP00000501603.1:n.942+19_942+20insACATT
ENST00000676439.1:n.1116+19_1116+20insACATT
ENST00000251127.10:c.942+19_942+20insACATT	ENSP00000251127.6:n.942+19_942+20insACATT
ENST00000470333.1:n.1038+19_1038+20insACATT
ENST00000497170.5:n.1096+19_1096+20insACATT
NM_052867.2:c.942+19_942+20insACATT	NP_443099.1:n.942+19_942+20insACATT
XM_011521067.1:c.999+19_999+20insACATT	XP_011519369.1:n.999+19_999+20insACATT
XM_011521068.1:c.942+19_942+20insACATT	XP_011519370.1:n.942+19_942+20insACATT
XM_011521069.1:c.999+19_999+20insACATT	XP_011519371.1:n.999+19_999+20insACATT
XM_011521070.1:c.999+19_999+20insACATT	XP_011519372.1:n.999+19_999+20insACATT
NM_001350748.1:c.942+19_942+20insACATT	NP_001337677.1:n.942+19_942+20insACATT
NM_001350749.1:c.942+19_942+20insACATT	NP_001337678.1:n.942+19_942+20insACATT
NM_001350750.1:c.942+19_942+20insACATT	NP_001337679.1:n.942+19_942+20insACATT
NM_001350751.1:c.942+19_942+20insACATT	NP_001337680.1:n.942+19_942+20insACATT
NM_052867.3:c.942+19_942+20insACATT	NP_443099.1:n.942+19_942+20insACATT
XM_011521067.2:c.999+19_999+20insACATT	XP_011519369.1:n.999+19_999+20insACATT
XM_011521069.2:c.999+19_999+20insACATT	XP_011519371.1:n.999+19_999+20insACATT
XM_017020536.2:c.495+19_495+20insACATT	XP_016876025.1:n.495+19_495+20insACATT
XM_017020537.1:c.177+19_177+20insACATT	XP_016876026.1:n.177+19_177+20insACATT
XM_024449336.1:c.999+19_999+20insACATT	XP_024305104.1:n.999+19_999+20insACATT
NM_052867.4:c.942+19_942+20insACATT MANE Select	NP_443099.1:n.942+19_942+20insACATT
NM_001350748.2:c.942+19_942+20insACATT	NP_001337677.1:n.942+19_942+20insACATT
NM_001350749.2:c.942+19_942+20insACATT	NP_001337678.1:n.942+19_942+20insACATT
NM_001350750.2:c.942+19_942+20insACATT	NP_001337679.1:n.942+19_942+20insACATT
NM_001350751.2:c.942+19_942+20insACATT	NP_001337680.1:n.942+19_942+20insACATT