Canonical Allele Identifier: CA2114379268

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101060838_101060841delinsAGAG , CM000675.2:g.101060838_101060841delinsAGAG	GRCh38
NC_000013.10:g.101713190_101713193delinsAGAG , CM000675.1:g.101713190_101713193delinsAGAG	GRCh37
NC_000013.9:g.100511191_100511194delinsAGAG	NCBI36
NG_053176.1:g.361366_361369delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4756-874_4756-871delinsCTCT MANE Select	ENSP00000251127.6:n.4756-874_4756-871delinsCTCT
ENST00000648359.1:c.*376-874_*376-871delinsCTCT	ENSP00000497465.1:n.*376-874_*376-871delinsCTCT
ENST00000675150.1:c.4477-874_4477-871delinsCTCT	ENSP00000502680.1:n.4477-874_4477-871delinsCTCT
ENST00000675332.1:c.4843-874_4843-871delinsCTCT	ENSP00000501955.1:n.4843-874_4843-871delinsCTCT
ENST00000676315.1:c.4669-874_4669-871delinsCTCT	ENSP00000501603.1:n.4669-874_4669-871delinsCTCT
ENST00000251127.10:c.4756-874_4756-871delinsCTCT	ENSP00000251127.6:n.4756-874_4756-871delinsCTCT
NM_052867.2:c.4756-874_4756-871delinsCTCT	NP_443099.1:n.4756-874_4756-871delinsCTCT
XM_011521067.1:c.4813-874_4813-871delinsCTCT	XP_011519369.1:n.4813-874_4813-871delinsCTCT
XM_011521068.1:c.4756-874_4756-871delinsCTCT	XP_011519370.1:n.4756-874_4756-871delinsCTCT
XM_011521069.1:c.4726-874_4726-871delinsCTCT	XP_011519371.1:n.4726-874_4726-871delinsCTCT
XM_011521070.1:c.4534-874_4534-871delinsCTCT	XP_011519372.1:n.4534-874_4534-871delinsCTCT
NM_001350748.1:c.4843-874_4843-871delinsCTCT	NP_001337677.1:n.4843-874_4843-871delinsCTCT
NM_001350749.1:c.4756-874_4756-871delinsCTCT	NP_001337678.1:n.4756-874_4756-871delinsCTCT
NM_001350750.1:c.4669-874_4669-871delinsCTCT	NP_001337679.1:n.4669-874_4669-871delinsCTCT
NM_001350751.1:c.4669-874_4669-871delinsCTCT	NP_001337680.1:n.4669-874_4669-871delinsCTCT
NM_052867.3:c.4756-874_4756-871delinsCTCT	NP_443099.1:n.4756-874_4756-871delinsCTCT
XM_011521067.2:c.4813-874_4813-871delinsCTCT	XP_011519369.1:n.4813-874_4813-871delinsCTCT
XM_011521069.2:c.4726-874_4726-871delinsCTCT	XP_011519371.1:n.4726-874_4726-871delinsCTCT
XM_017020536.2:c.4309-874_4309-871delinsCTCT	XP_016876025.1:n.4309-874_4309-871delinsCTCT
XM_017020537.1:c.3991-874_3991-871delinsCTCT	XP_016876026.1:n.3991-874_3991-871delinsCTCT
XM_024449336.1:c.4900-874_4900-871delinsCTCT	XP_024305104.1:n.4900-874_4900-871delinsCTCT
NM_052867.4:c.4756-874_4756-871delinsCTCT MANE Select	NP_443099.1:n.4756-874_4756-871delinsCTCT
NM_001350748.2:c.4843-874_4843-871delinsCTCT	NP_001337677.1:n.4843-874_4843-871delinsCTCT
NM_001350749.2:c.4756-874_4756-871delinsCTCT	NP_001337678.1:n.4756-874_4756-871delinsCTCT
NM_001350750.2:c.4669-874_4669-871delinsCTCT	NP_001337679.1:n.4669-874_4669-871delinsCTCT
NM_001350751.2:c.4669-874_4669-871delinsCTCT	NP_001337680.1:n.4669-874_4669-871delinsCTCT