Canonical Allele Identifier: CA959531184

Gene: NALCN

Linked Data

• gnomAD v3: 13-101061076-TGTGA-T
• gnomAD v4: 13-101061076-TGTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101061077_101061080del , CM000675.2:g.101061077_101061080del	GRCh38
NC_000013.10:g.101713429_101713432del , CM000675.1:g.101713429_101713432del	GRCh37
NC_000013.9:g.100511430_100511433del	NCBI36
NG_053176.1:g.361127_361130del

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.4755+888_4755+891del MANE Select	ENSP00000251127.6:n.4755+888_4755+891del
ENST00000648359.1:c.*375+888_*375+891del	ENSP00000497465.1:n.*375+888_*375+891del
ENST00000675150.1:c.4476+888_4476+891del	ENSP00000502680.1:n.4476+888_4476+891del
ENST00000675332.1:c.4842+888_4842+891del	ENSP00000501955.1:n.4842+888_4842+891del
ENST00000676315.1:c.4668+888_4668+891del	ENSP00000501603.1:n.4668+888_4668+891del
ENST00000251127.10:c.4755+888_4755+891del	ENSP00000251127.6:n.4755+888_4755+891del
NM_052867.2:c.4755+888_4755+891del	NP_443099.1:n.4755+888_4755+891del
XM_011521067.1:c.4812+888_4812+891del	XP_011519369.1:n.4812+888_4812+891del
XM_011521068.1:c.4755+888_4755+891del	XP_011519370.1:n.4755+888_4755+891del
XM_011521069.1:c.4725+888_4725+891del	XP_011519371.1:n.4725+888_4725+891del
XM_011521070.1:c.4533+888_4533+891del	XP_011519372.1:n.4533+888_4533+891del
NM_001350748.1:c.4842+888_4842+891del	NP_001337677.1:n.4842+888_4842+891del
NM_001350749.1:c.4755+888_4755+891del	NP_001337678.1:n.4755+888_4755+891del
NM_001350750.1:c.4668+888_4668+891del	NP_001337679.1:n.4668+888_4668+891del
NM_001350751.1:c.4668+888_4668+891del	NP_001337680.1:n.4668+888_4668+891del
NM_052867.3:c.4755+888_4755+891del	NP_443099.1:n.4755+888_4755+891del
XM_011521067.2:c.4812+888_4812+891del	XP_011519369.1:n.4812+888_4812+891del
XM_011521069.2:c.4725+888_4725+891del	XP_011519371.1:n.4725+888_4725+891del
XM_017020536.2:c.4308+888_4308+891del	XP_016876025.1:n.4308+888_4308+891del
XM_017020537.1:c.3990+888_3990+891del	XP_016876026.1:n.3990+888_3990+891del
XM_024449336.1:c.4899+888_4899+891del	XP_024305104.1:n.4899+888_4899+891del
NM_052867.4:c.4755+888_4755+891del MANE Select	NP_443099.1:n.4755+888_4755+891del
NM_001350748.2:c.4842+888_4842+891del	NP_001337677.1:n.4842+888_4842+891del
NM_001350749.2:c.4755+888_4755+891del	NP_001337678.1:n.4755+888_4755+891del
NM_001350750.2:c.4668+888_4668+891del	NP_001337679.1:n.4668+888_4668+891del
NM_001350751.2:c.4668+888_4668+891del	NP_001337680.1:n.4668+888_4668+891del