Canonical Allele Identifier: CA7035269

Gene: NALCN

Linked Data

• dbSNP Id: rs754064143
• ExAC: 13:101733858 AACTTG / A
• gnomAD v2: 13-101733858-AACTTG-A
• gnomAD v3: 13-101081507-AACTTG-A
• gnomAD v4: 13-101081507-AACTTG-A
• MyVariant Identifiers: chr13:g.101733859_101733863del (hg19) ; chr13:g.101081508_101081512del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081512_101081516del , CM000675.2:g.101081512_101081516del	GRCh38
NC_000013.10:g.101733863_101733867del , CM000675.1:g.101733863_101733867del	GRCh37
NC_000013.9:g.100531864_100531868del	NCBI36
NG_053176.1:g.340695_340699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3885+15_3885+19del MANE Select	ENSP00000251127.6:n.3885+15_3885+19del
ENST00000648359.1:c.3885+15_3885+19del	ENSP00000497465.1:n.3885+15_3885+19del
ENST00000675150.1:c.3606+15_3606+19del	ENSP00000502680.1:n.3606+15_3606+19del
ENST00000675332.1:c.3972+15_3972+19del	ENSP00000501955.1:n.3972+15_3972+19del
ENST00000676315.1:c.3798+15_3798+19del	ENSP00000501603.1:n.3798+15_3798+19del
ENST00000251127.10:c.3885+15_3885+19del	ENSP00000251127.6:n.3885+15_3885+19del
NM_052867.2:c.3885+15_3885+19del	NP_443099.1:n.3885+15_3885+19del
XM_011521067.1:c.3942+15_3942+19del	XP_011519369.1:n.3942+15_3942+19del
XM_011521068.1:c.3885+15_3885+19del	XP_011519370.1:n.3885+15_3885+19del
XM_011521069.1:c.3855+15_3855+19del	XP_011519371.1:n.3855+15_3855+19del
XM_011521070.1:c.3663+15_3663+19del	XP_011519372.1:n.3663+15_3663+19del
NM_001350748.1:c.3972+15_3972+19del	NP_001337677.1:n.3972+15_3972+19del
NM_001350749.1:c.3885+15_3885+19del	NP_001337678.1:n.3885+15_3885+19del
NM_001350750.1:c.3798+15_3798+19del	NP_001337679.1:n.3798+15_3798+19del
NM_001350751.1:c.3798+15_3798+19del	NP_001337680.1:n.3798+15_3798+19del
NM_052867.3:c.3885+15_3885+19del	NP_443099.1:n.3885+15_3885+19del
XM_011521067.2:c.3942+15_3942+19del	XP_011519369.1:n.3942+15_3942+19del
XM_011521069.2:c.3855+15_3855+19del	XP_011519371.1:n.3855+15_3855+19del
XM_017020536.2:c.3438+15_3438+19del	XP_016876025.1:n.3438+15_3438+19del
XM_017020537.1:c.3120+15_3120+19del	XP_016876026.1:n.3120+15_3120+19del
XM_024449336.1:c.4029+15_4029+19del	XP_024305104.1:n.4029+15_4029+19del
NM_052867.4:c.3885+15_3885+19del MANE Select	NP_443099.1:n.3885+15_3885+19del
NM_001350748.2:c.3972+15_3972+19del	NP_001337677.1:n.3972+15_3972+19del
NM_001350749.2:c.3885+15_3885+19del	NP_001337678.1:n.3885+15_3885+19del
NM_001350750.2:c.3798+15_3798+19del	NP_001337679.1:n.3798+15_3798+19del
NM_001350751.2:c.3798+15_3798+19del	NP_001337680.1:n.3798+15_3798+19del