Canonical Allele Identifier: CA611941190

Gene: NALCN

Linked Data

• dbSNP Id: rs1409598469
• gnomAD v2: 13-101713244-TGGGACATCACTGG-T
• gnomAD v3: 13-101060892-TGGGACATCACTGG-T
• gnomAD v4: 13-101060892-TGGGACATCACTGG-T
• MyVariant Identifiers: chr13:g.101713245_101713257del (hg19) ; chr13:g.101060893_101060905del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101060894_101060906del , CM000675.2:g.101060894_101060906del	GRCh38
NC_000013.10:g.101713246_101713258del , CM000675.1:g.101713246_101713258del	GRCh37
NC_000013.9:g.100511247_100511259del	NCBI36
NG_053176.1:g.361302_361314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4756-938_4756-926del MANE Select	ENSP00000251127.6:n.4756-938_4756-926del
ENST00000648359.1:c.*376-938_*376-926del	ENSP00000497465.1:n.*376-938_*376-926del
ENST00000675150.1:c.4477-938_4477-926del	ENSP00000502680.1:n.4477-938_4477-926del
ENST00000675332.1:c.4843-938_4843-926del	ENSP00000501955.1:n.4843-938_4843-926del
ENST00000676315.1:c.4669-938_4669-926del	ENSP00000501603.1:n.4669-938_4669-926del
ENST00000251127.10:c.4756-938_4756-926del	ENSP00000251127.6:n.4756-938_4756-926del
NM_052867.2:c.4756-938_4756-926del	NP_443099.1:n.4756-938_4756-926del
XM_011521067.1:c.4813-938_4813-926del	XP_011519369.1:n.4813-938_4813-926del
XM_011521068.1:c.4756-938_4756-926del	XP_011519370.1:n.4756-938_4756-926del
XM_011521069.1:c.4726-938_4726-926del	XP_011519371.1:n.4726-938_4726-926del
XM_011521070.1:c.4534-938_4534-926del	XP_011519372.1:n.4534-938_4534-926del
NM_001350748.1:c.4843-938_4843-926del	NP_001337677.1:n.4843-938_4843-926del
NM_001350749.1:c.4756-938_4756-926del	NP_001337678.1:n.4756-938_4756-926del
NM_001350750.1:c.4669-938_4669-926del	NP_001337679.1:n.4669-938_4669-926del
NM_001350751.1:c.4669-938_4669-926del	NP_001337680.1:n.4669-938_4669-926del
NM_052867.3:c.4756-938_4756-926del	NP_443099.1:n.4756-938_4756-926del
XM_011521067.2:c.4813-938_4813-926del	XP_011519369.1:n.4813-938_4813-926del
XM_011521069.2:c.4726-938_4726-926del	XP_011519371.1:n.4726-938_4726-926del
XM_017020536.2:c.4309-938_4309-926del	XP_016876025.1:n.4309-938_4309-926del
XM_017020537.1:c.3991-938_3991-926del	XP_016876026.1:n.3991-938_3991-926del
XM_024449336.1:c.4900-938_4900-926del	XP_024305104.1:n.4900-938_4900-926del
NM_052867.4:c.4756-938_4756-926del MANE Select	NP_443099.1:n.4756-938_4756-926del
NM_001350748.2:c.4843-938_4843-926del	NP_001337677.1:n.4843-938_4843-926del
NM_001350749.2:c.4756-938_4756-926del	NP_001337678.1:n.4756-938_4756-926del
NM_001350750.2:c.4669-938_4669-926del	NP_001337679.1:n.4669-938_4669-926del
NM_001350751.2:c.4669-938_4669-926del	NP_001337680.1:n.4669-938_4669-926del