Canonical Allele Identifier: CA2114483784

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101291886_101291887delinsTA , CM000675.2:g.101291886_101291887delinsTA	GRCh38
NC_000013.10:g.101944237_101944238delinsTA , CM000675.1:g.101944237_101944238delinsTA	GRCh37
NC_000013.9:g.100742238_100742239delinsTA	NCBI36
NG_053176.1:g.130320_130321delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.1047+103_1047+104delinsTA MANE Select	ENSP00000251127.6:n.1047+103_1047+104delinsTA
ENST00000648359.1:c.1047+103_1047+104delinsTA	ENSP00000497465.1:n.1047+103_1047+104delinsTA
ENST00000674840.1:n.1145+103_1145+104delinsTA
ENST00000674904.1:n.1127+103_1127+104delinsTA
ENST00000675150.1:c.1047+103_1047+104delinsTA	ENSP00000502680.1:n.1047+103_1047+104delinsTA
ENST00000675332.1:c.1047+103_1047+104delinsTA	ENSP00000501955.1:n.1047+103_1047+104delinsTA
ENST00000675415.1:n.1230+103_1230+104delinsTA
ENST00000675594.1:c.*484+103_*484+104delinsTA	ENSP00000502490.1:n.*484+103_*484+104delinsTA
ENST00000675802.1:c.1047+103_1047+104delinsTA	ENSP00000501818.1:n.1047+103_1047+104delinsTA
ENST00000676315.1:c.1047+103_1047+104delinsTA	ENSP00000501603.1:n.1047+103_1047+104delinsTA
ENST00000676439.1:n.1221+103_1221+104delinsTA
ENST00000251127.10:c.1047+103_1047+104delinsTA	ENSP00000251127.6:n.1047+103_1047+104delinsTA
ENST00000470333.1:n.1143+103_1143+104delinsTA
ENST00000497170.5:n.1201+103_1201+104delinsTA
NM_052867.2:c.1047+103_1047+104delinsTA	NP_443099.1:n.1047+103_1047+104delinsTA
XM_011521067.1:c.1104+103_1104+104delinsTA	XP_011519369.1:n.1104+103_1104+104delinsTA
XM_011521068.1:c.1047+103_1047+104delinsTA	XP_011519370.1:n.1047+103_1047+104delinsTA
XM_011521069.1:c.1104+103_1104+104delinsTA	XP_011519371.1:n.1104+103_1104+104delinsTA
XM_011521070.1:c.1104+103_1104+104delinsTA	XP_011519372.1:n.1104+103_1104+104delinsTA
NM_001350748.1:c.1047+103_1047+104delinsTA	NP_001337677.1:n.1047+103_1047+104delinsTA
NM_001350749.1:c.1047+103_1047+104delinsTA	NP_001337678.1:n.1047+103_1047+104delinsTA
NM_001350750.1:c.1047+103_1047+104delinsTA	NP_001337679.1:n.1047+103_1047+104delinsTA
NM_001350751.1:c.1047+103_1047+104delinsTA	NP_001337680.1:n.1047+103_1047+104delinsTA
NM_052867.3:c.1047+103_1047+104delinsTA	NP_443099.1:n.1047+103_1047+104delinsTA
XM_011521067.2:c.1104+103_1104+104delinsTA	XP_011519369.1:n.1104+103_1104+104delinsTA
XM_011521069.2:c.1104+103_1104+104delinsTA	XP_011519371.1:n.1104+103_1104+104delinsTA
XM_017020536.2:c.600+103_600+104delinsTA	XP_016876025.1:n.600+103_600+104delinsTA
XM_017020537.1:c.282+103_282+104delinsTA	XP_016876026.1:n.282+103_282+104delinsTA
XM_024449336.1:c.1104+103_1104+104delinsTA	XP_024305104.1:n.1104+103_1104+104delinsTA
NM_052867.4:c.1047+103_1047+104delinsTA MANE Select	NP_443099.1:n.1047+103_1047+104delinsTA
NM_001350748.2:c.1047+103_1047+104delinsTA	NP_001337677.1:n.1047+103_1047+104delinsTA
NM_001350749.2:c.1047+103_1047+104delinsTA	NP_001337678.1:n.1047+103_1047+104delinsTA
NM_001350750.2:c.1047+103_1047+104delinsTA	NP_001337679.1:n.1047+103_1047+104delinsTA
NM_001350751.2:c.1047+103_1047+104delinsTA	NP_001337680.1:n.1047+103_1047+104delinsTA