Canonical Allele Identifier: CA2623583378

Gene: NALCN

Linked Data

• gnomAD v4: 13-101291943-A-ACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101291943_101291944insCCC , CM000675.2:g.101291943_101291944insCCC	GRCh38
NC_000013.10:g.101944294_101944295insCCC , CM000675.1:g.101944294_101944295insCCC	GRCh37
NC_000013.9:g.100742295_100742296insCCC	NCBI36
NG_053176.1:g.130263_130264insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.1047+46_1047+47insGGG MANE Select	ENSP00000251127.6:n.1047+46_1047+47insGGG
ENST00000648359.1:c.1047+46_1047+47insGGG	ENSP00000497465.1:n.1047+46_1047+47insGGG
ENST00000674840.1:n.1145+46_1145+47insGGG
ENST00000674904.1:n.1127+46_1127+47insGGG
ENST00000675150.1:c.1047+46_1047+47insGGG	ENSP00000502680.1:n.1047+46_1047+47insGGG
ENST00000675332.1:c.1047+46_1047+47insGGG	ENSP00000501955.1:n.1047+46_1047+47insGGG
ENST00000675415.1:n.1230+46_1230+47insGGG
ENST00000675594.1:c.*484+46_*484+47insGGG	ENSP00000502490.1:n.*484+46_*484+47insGGG
ENST00000675802.1:c.1047+46_1047+47insGGG	ENSP00000501818.1:n.1047+46_1047+47insGGG
ENST00000676315.1:c.1047+46_1047+47insGGG	ENSP00000501603.1:n.1047+46_1047+47insGGG
ENST00000676439.1:n.1221+46_1221+47insGGG
ENST00000251127.10:c.1047+46_1047+47insGGG	ENSP00000251127.6:n.1047+46_1047+47insGGG
ENST00000470333.1:n.1143+46_1143+47insGGG
ENST00000497170.5:n.1201+46_1201+47insGGG
NM_052867.2:c.1047+46_1047+47insGGG	NP_443099.1:n.1047+46_1047+47insGGG
XM_011521067.1:c.1104+46_1104+47insGGG	XP_011519369.1:n.1104+46_1104+47insGGG
XM_011521068.1:c.1047+46_1047+47insGGG	XP_011519370.1:n.1047+46_1047+47insGGG
XM_011521069.1:c.1104+46_1104+47insGGG	XP_011519371.1:n.1104+46_1104+47insGGG
XM_011521070.1:c.1104+46_1104+47insGGG	XP_011519372.1:n.1104+46_1104+47insGGG
NM_001350748.1:c.1047+46_1047+47insGGG	NP_001337677.1:n.1047+46_1047+47insGGG
NM_001350749.1:c.1047+46_1047+47insGGG	NP_001337678.1:n.1047+46_1047+47insGGG
NM_001350750.1:c.1047+46_1047+47insGGG	NP_001337679.1:n.1047+46_1047+47insGGG
NM_001350751.1:c.1047+46_1047+47insGGG	NP_001337680.1:n.1047+46_1047+47insGGG
NM_052867.3:c.1047+46_1047+47insGGG	NP_443099.1:n.1047+46_1047+47insGGG
XM_011521067.2:c.1104+46_1104+47insGGG	XP_011519369.1:n.1104+46_1104+47insGGG
XM_011521069.2:c.1104+46_1104+47insGGG	XP_011519371.1:n.1104+46_1104+47insGGG
XM_017020536.2:c.600+46_600+47insGGG	XP_016876025.1:n.600+46_600+47insGGG
XM_017020537.1:c.282+46_282+47insGGG	XP_016876026.1:n.282+46_282+47insGGG
XM_024449336.1:c.1104+46_1104+47insGGG	XP_024305104.1:n.1104+46_1104+47insGGG
NM_052867.4:c.1047+46_1047+47insGGG MANE Select	NP_443099.1:n.1047+46_1047+47insGGG
NM_001350748.2:c.1047+46_1047+47insGGG	NP_001337677.1:n.1047+46_1047+47insGGG
NM_001350749.2:c.1047+46_1047+47insGGG	NP_001337678.1:n.1047+46_1047+47insGGG
NM_001350750.2:c.1047+46_1047+47insGGG	NP_001337679.1:n.1047+46_1047+47insGGG
NM_001350751.2:c.1047+46_1047+47insGGG	NP_001337680.1:n.1047+46_1047+47insGGG