Canonical Allele Identifier: CA2623583393

Gene: NALCN

Linked Data

• gnomAD v4: 13-101291962-TTATAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101291963_101291967del , CM000675.2:g.101291963_101291967del	GRCh38
NC_000013.10:g.101944314_101944318del , CM000675.1:g.101944314_101944318del	GRCh37
NC_000013.9:g.100742315_100742319del	NCBI36
NG_053176.1:g.130240_130244del

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1047+23_1047+27del MANE Select	ENSP00000251127.6:n.1047+23_1047+27del
ENST00000648359.1:c.1047+23_1047+27del	ENSP00000497465.1:n.1047+23_1047+27del
ENST00000674840.1:n.1145+23_1145+27del
ENST00000674904.1:n.1127+23_1127+27del
ENST00000675150.1:c.1047+23_1047+27del	ENSP00000502680.1:n.1047+23_1047+27del
ENST00000675332.1:c.1047+23_1047+27del	ENSP00000501955.1:n.1047+23_1047+27del
ENST00000675415.1:n.1230+23_1230+27del
ENST00000675594.1:c.*484+23_*484+27del	ENSP00000502490.1:n.*484+23_*484+27del
ENST00000675802.1:c.1047+23_1047+27del	ENSP00000501818.1:n.1047+23_1047+27del
ENST00000676315.1:c.1047+23_1047+27del	ENSP00000501603.1:n.1047+23_1047+27del
ENST00000676439.1:n.1221+23_1221+27del
ENST00000251127.10:c.1047+23_1047+27del	ENSP00000251127.6:n.1047+23_1047+27del
ENST00000470333.1:n.1143+23_1143+27del
ENST00000497170.5:n.1201+23_1201+27del
NM_052867.2:c.1047+23_1047+27del	NP_443099.1:n.1047+23_1047+27del
XM_011521067.1:c.1104+23_1104+27del	XP_011519369.1:n.1104+23_1104+27del
XM_011521068.1:c.1047+23_1047+27del	XP_011519370.1:n.1047+23_1047+27del
XM_011521069.1:c.1104+23_1104+27del	XP_011519371.1:n.1104+23_1104+27del
XM_011521070.1:c.1104+23_1104+27del	XP_011519372.1:n.1104+23_1104+27del
NM_001350748.1:c.1047+23_1047+27del	NP_001337677.1:n.1047+23_1047+27del
NM_001350749.1:c.1047+23_1047+27del	NP_001337678.1:n.1047+23_1047+27del
NM_001350750.1:c.1047+23_1047+27del	NP_001337679.1:n.1047+23_1047+27del
NM_001350751.1:c.1047+23_1047+27del	NP_001337680.1:n.1047+23_1047+27del
NM_052867.3:c.1047+23_1047+27del	NP_443099.1:n.1047+23_1047+27del
XM_011521067.2:c.1104+23_1104+27del	XP_011519369.1:n.1104+23_1104+27del
XM_011521069.2:c.1104+23_1104+27del	XP_011519371.1:n.1104+23_1104+27del
XM_017020536.2:c.600+23_600+27del	XP_016876025.1:n.600+23_600+27del
XM_017020537.1:c.282+23_282+27del	XP_016876026.1:n.282+23_282+27del
XM_024449336.1:c.1104+23_1104+27del	XP_024305104.1:n.1104+23_1104+27del
NM_052867.4:c.1047+23_1047+27del MANE Select	NP_443099.1:n.1047+23_1047+27del
NM_001350748.2:c.1047+23_1047+27del	NP_001337677.1:n.1047+23_1047+27del
NM_001350749.2:c.1047+23_1047+27del	NP_001337678.1:n.1047+23_1047+27del
NM_001350750.2:c.1047+23_1047+27del	NP_001337679.1:n.1047+23_1047+27del
NM_001350751.2:c.1047+23_1047+27del	NP_001337680.1:n.1047+23_1047+27del