Canonical Allele Identifier: CA959542086

Gene: NALCN

Linked Data

• dbSNP Id: rs2033674091
• gnomAD v3: 13-101081903-AGTCTCGCTCT-A
• gnomAD v4: 13-101081903-AGTCTCGCTCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081907_101081916del , CM000675.2:g.101081907_101081916del	GRCh38
NC_000013.10:g.101734258_101734267del , CM000675.1:g.101734258_101734267del	GRCh37
NC_000013.9:g.100532259_100532268del	NCBI36
NG_053176.1:g.340294_340303del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3766-267_3766-258del MANE Select	ENSP00000251127.6:n.3766-267_3766-258del
ENST00000648359.1:c.3766-267_3766-258del	ENSP00000497465.1:n.3766-267_3766-258del
ENST00000675150.1:c.3487-267_3487-258del	ENSP00000502680.1:n.3487-267_3487-258del
ENST00000675332.1:c.3853-267_3853-258del	ENSP00000501955.1:n.3853-267_3853-258del
ENST00000676315.1:c.3679-267_3679-258del	ENSP00000501603.1:n.3679-267_3679-258del
ENST00000251127.10:c.3766-267_3766-258del	ENSP00000251127.6:n.3766-267_3766-258del
NM_052867.2:c.3766-267_3766-258del	NP_443099.1:n.3766-267_3766-258del
XM_011521067.1:c.3823-267_3823-258del	XP_011519369.1:n.3823-267_3823-258del
XM_011521068.1:c.3766-267_3766-258del	XP_011519370.1:n.3766-267_3766-258del
XM_011521069.1:c.3736-267_3736-258del	XP_011519371.1:n.3736-267_3736-258del
XM_011521070.1:c.3544-267_3544-258del	XP_011519372.1:n.3544-267_3544-258del
NM_001350748.1:c.3853-267_3853-258del	NP_001337677.1:n.3853-267_3853-258del
NM_001350749.1:c.3766-267_3766-258del	NP_001337678.1:n.3766-267_3766-258del
NM_001350750.1:c.3679-267_3679-258del	NP_001337679.1:n.3679-267_3679-258del
NM_001350751.1:c.3679-267_3679-258del	NP_001337680.1:n.3679-267_3679-258del
NM_052867.3:c.3766-267_3766-258del	NP_443099.1:n.3766-267_3766-258del
XM_011521067.2:c.3823-267_3823-258del	XP_011519369.1:n.3823-267_3823-258del
XM_011521069.2:c.3736-267_3736-258del	XP_011519371.1:n.3736-267_3736-258del
XM_017020536.2:c.3319-267_3319-258del	XP_016876025.1:n.3319-267_3319-258del
XM_017020537.1:c.3001-267_3001-258del	XP_016876026.1:n.3001-267_3001-258del
XM_024449336.1:c.3910-267_3910-258del	XP_024305104.1:n.3910-267_3910-258del
NM_052867.4:c.3766-267_3766-258del MANE Select	NP_443099.1:n.3766-267_3766-258del
NM_001350748.2:c.3853-267_3853-258del	NP_001337677.1:n.3853-267_3853-258del
NM_001350749.2:c.3766-267_3766-258del	NP_001337678.1:n.3766-267_3766-258del
NM_001350750.2:c.3679-267_3679-258del	NP_001337679.1:n.3679-267_3679-258del
NM_001350751.2:c.3679-267_3679-258del	NP_001337680.1:n.3679-267_3679-258del