Canonical Allele Identifier: CA2114388780

Gene: NALCN

Linked Data

• dbSNP Id: rs2033642600
• gnomAD v4: 13-101081412-CATCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081414_101081417del , CM000675.2:g.101081414_101081417del	GRCh38
NC_000013.10:g.101733765_101733768del , CM000675.1:g.101733765_101733768del	GRCh37
NC_000013.9:g.100531766_100531769del	NCBI36
NG_053176.1:g.340791_340794del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3885+111_3885+114del MANE Select	ENSP00000251127.6:n.3885+111_3885+114del
ENST00000648359.1:c.3885+111_3885+114del	ENSP00000497465.1:n.3885+111_3885+114del
ENST00000675150.1:c.3606+111_3606+114del	ENSP00000502680.1:n.3606+111_3606+114del
ENST00000675332.1:c.3972+111_3972+114del	ENSP00000501955.1:n.3972+111_3972+114del
ENST00000676315.1:c.3798+111_3798+114del	ENSP00000501603.1:n.3798+111_3798+114del
ENST00000251127.10:c.3885+111_3885+114del	ENSP00000251127.6:n.3885+111_3885+114del
NM_052867.2:c.3885+111_3885+114del	NP_443099.1:n.3885+111_3885+114del
XM_011521067.1:c.3942+111_3942+114del	XP_011519369.1:n.3942+111_3942+114del
XM_011521068.1:c.3885+111_3885+114del	XP_011519370.1:n.3885+111_3885+114del
XM_011521069.1:c.3855+111_3855+114del	XP_011519371.1:n.3855+111_3855+114del
XM_011521070.1:c.3663+111_3663+114del	XP_011519372.1:n.3663+111_3663+114del
NM_001350748.1:c.3972+111_3972+114del	NP_001337677.1:n.3972+111_3972+114del
NM_001350749.1:c.3885+111_3885+114del	NP_001337678.1:n.3885+111_3885+114del
NM_001350750.1:c.3798+111_3798+114del	NP_001337679.1:n.3798+111_3798+114del
NM_001350751.1:c.3798+111_3798+114del	NP_001337680.1:n.3798+111_3798+114del
NM_052867.3:c.3885+111_3885+114del	NP_443099.1:n.3885+111_3885+114del
XM_011521067.2:c.3942+111_3942+114del	XP_011519369.1:n.3942+111_3942+114del
XM_011521069.2:c.3855+111_3855+114del	XP_011519371.1:n.3855+111_3855+114del
XM_017020536.2:c.3438+111_3438+114del	XP_016876025.1:n.3438+111_3438+114del
XM_017020537.1:c.3120+111_3120+114del	XP_016876026.1:n.3120+111_3120+114del
XM_024449336.1:c.4029+111_4029+114del	XP_024305104.1:n.4029+111_4029+114del
NM_052867.4:c.3885+111_3885+114del MANE Select	NP_443099.1:n.3885+111_3885+114del
NM_001350748.2:c.3972+111_3972+114del	NP_001337677.1:n.3972+111_3972+114del
NM_001350749.2:c.3885+111_3885+114del	NP_001337678.1:n.3885+111_3885+114del
NM_001350750.2:c.3798+111_3798+114del	NP_001337679.1:n.3798+111_3798+114del
NM_001350751.2:c.3798+111_3798+114del	NP_001337680.1:n.3798+111_3798+114del