Canonical Allele Identifier: CA694196609

Gene: NALCN

Linked Data

• dbSNP Id: rs1306066882
• gnomAD v3: 13-101061008-GGAA-G
• gnomAD v4: 13-101061008-GGAA-G
• MyVariant Identifiers: chr13:g.101713361_101713363del (hg19) ; chr13:g.101061009_101061011del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101061011_101061013del , CM000675.2:g.101061011_101061013del	GRCh38
NC_000013.10:g.101713363_101713365del , CM000675.1:g.101713363_101713365del	GRCh37
NC_000013.9:g.100511364_100511366del	NCBI36
NG_053176.1:g.361196_361198del

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.4755+957_4755+959del MANE Select	ENSP00000251127.6:n.4755+957_4755+959del
ENST00000648359.1:c.*375+957_*375+959del	ENSP00000497465.1:n.*375+957_*375+959del
ENST00000675150.1:c.4476+957_4476+959del	ENSP00000502680.1:n.4476+957_4476+959del
ENST00000675332.1:c.4842+957_4842+959del	ENSP00000501955.1:n.4842+957_4842+959del
ENST00000676315.1:c.4668+957_4668+959del	ENSP00000501603.1:n.4668+957_4668+959del
ENST00000251127.10:c.4755+957_4755+959del	ENSP00000251127.6:n.4755+957_4755+959del
NM_052867.2:c.4755+957_4755+959del	NP_443099.1:n.4755+957_4755+959del
XM_011521067.1:c.4812+957_4812+959del	XP_011519369.1:n.4812+957_4812+959del
XM_011521068.1:c.4755+957_4755+959del	XP_011519370.1:n.4755+957_4755+959del
XM_011521069.1:c.4725+957_4725+959del	XP_011519371.1:n.4725+957_4725+959del
XM_011521070.1:c.4533+957_4533+959del	XP_011519372.1:n.4533+957_4533+959del
NM_001350748.1:c.4842+957_4842+959del	NP_001337677.1:n.4842+957_4842+959del
NM_001350749.1:c.4755+957_4755+959del	NP_001337678.1:n.4755+957_4755+959del
NM_001350750.1:c.4668+957_4668+959del	NP_001337679.1:n.4668+957_4668+959del
NM_001350751.1:c.4668+957_4668+959del	NP_001337680.1:n.4668+957_4668+959del
NM_052867.3:c.4755+957_4755+959del	NP_443099.1:n.4755+957_4755+959del
XM_011521067.2:c.4812+957_4812+959del	XP_011519369.1:n.4812+957_4812+959del
XM_011521069.2:c.4725+957_4725+959del	XP_011519371.1:n.4725+957_4725+959del
XM_017020536.2:c.4308+957_4308+959del	XP_016876025.1:n.4308+957_4308+959del
XM_017020537.1:c.3990+957_3990+959del	XP_016876026.1:n.3990+957_3990+959del
XM_024449336.1:c.4899+957_4899+959del	XP_024305104.1:n.4899+957_4899+959del
NM_052867.4:c.4755+957_4755+959del MANE Select	NP_443099.1:n.4755+957_4755+959del
NM_001350748.2:c.4842+957_4842+959del	NP_001337677.1:n.4842+957_4842+959del
NM_001350749.2:c.4755+957_4755+959del	NP_001337678.1:n.4755+957_4755+959del
NM_001350750.2:c.4668+957_4668+959del	NP_001337679.1:n.4668+957_4668+959del
NM_001350751.2:c.4668+957_4668+959del	NP_001337680.1:n.4668+957_4668+959del