Canonical Allele Identifier: CA2114379382

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101061102_101061106delinsAAAGT , CM000675.2:g.101061102_101061106delinsAAAGT	GRCh38
NC_000013.10:g.101713454_101713458delinsAAAGT , CM000675.1:g.101713454_101713458delinsAAAGT	GRCh37
NC_000013.9:g.100511455_100511459delinsAAAGT	NCBI36
NG_053176.1:g.361101_361105delinsACTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4755+862_4755+866delinsACTTT MANE Select	ENSP00000251127.6:n.4755+862_4755+866delinsACTTT
ENST00000648359.1:c.*375+862_*375+866delinsACTTT	ENSP00000497465.1:n.*375+862_*375+866delinsACTTT
ENST00000675150.1:c.4476+862_4476+866delinsACTTT	ENSP00000502680.1:n.4476+862_4476+866delinsACTTT
ENST00000675332.1:c.4842+862_4842+866delinsACTTT	ENSP00000501955.1:n.4842+862_4842+866delinsACTTT
ENST00000676315.1:c.4668+862_4668+866delinsACTTT	ENSP00000501603.1:n.4668+862_4668+866delinsACTTT
ENST00000251127.10:c.4755+862_4755+866delinsACTTT	ENSP00000251127.6:n.4755+862_4755+866delinsACTTT
NM_052867.2:c.4755+862_4755+866delinsACTTT	NP_443099.1:n.4755+862_4755+866delinsACTTT
XM_011521067.1:c.4812+862_4812+866delinsACTTT	XP_011519369.1:n.4812+862_4812+866delinsACTTT
XM_011521068.1:c.4755+862_4755+866delinsACTTT	XP_011519370.1:n.4755+862_4755+866delinsACTTT
XM_011521069.1:c.4725+862_4725+866delinsACTTT	XP_011519371.1:n.4725+862_4725+866delinsACTTT
XM_011521070.1:c.4533+862_4533+866delinsACTTT	XP_011519372.1:n.4533+862_4533+866delinsACTTT
NM_001350748.1:c.4842+862_4842+866delinsACTTT	NP_001337677.1:n.4842+862_4842+866delinsACTTT
NM_001350749.1:c.4755+862_4755+866delinsACTTT	NP_001337678.1:n.4755+862_4755+866delinsACTTT
NM_001350750.1:c.4668+862_4668+866delinsACTTT	NP_001337679.1:n.4668+862_4668+866delinsACTTT
NM_001350751.1:c.4668+862_4668+866delinsACTTT	NP_001337680.1:n.4668+862_4668+866delinsACTTT
NM_052867.3:c.4755+862_4755+866delinsACTTT	NP_443099.1:n.4755+862_4755+866delinsACTTT
XM_011521067.2:c.4812+862_4812+866delinsACTTT	XP_011519369.1:n.4812+862_4812+866delinsACTTT
XM_011521069.2:c.4725+862_4725+866delinsACTTT	XP_011519371.1:n.4725+862_4725+866delinsACTTT
XM_017020536.2:c.4308+862_4308+866delinsACTTT	XP_016876025.1:n.4308+862_4308+866delinsACTTT
XM_017020537.1:c.3990+862_3990+866delinsACTTT	XP_016876026.1:n.3990+862_3990+866delinsACTTT
XM_024449336.1:c.4899+862_4899+866delinsACTTT	XP_024305104.1:n.4899+862_4899+866delinsACTTT
NM_052867.4:c.4755+862_4755+866delinsACTTT MANE Select	NP_443099.1:n.4755+862_4755+866delinsACTTT
NM_001350748.2:c.4842+862_4842+866delinsACTTT	NP_001337677.1:n.4842+862_4842+866delinsACTTT
NM_001350749.2:c.4755+862_4755+866delinsACTTT	NP_001337678.1:n.4755+862_4755+866delinsACTTT
NM_001350750.2:c.4668+862_4668+866delinsACTTT	NP_001337679.1:n.4668+862_4668+866delinsACTTT
NM_001350751.2:c.4668+862_4668+866delinsACTTT	NP_001337680.1:n.4668+862_4668+866delinsACTTT