Canonical Allele Identifier: CA256083010

Gene: NALCN

Linked Data

• dbSNP Id: rs533014706
• gnomAD v3: 13-101398840-AACTCATAGCG-A
• gnomAD v4: 13-101398840-AACTCATAGCG-A
• MyVariant Identifiers: chr13:g.102051192_102051201del (hg19) ; chr13:g.101398841_101398850del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101398843_101398852del , CM000675.2:g.101398843_101398852del	GRCh38
NC_000013.10:g.102051194_102051203del , CM000675.1:g.102051194_102051203del	GRCh37
NC_000013.9:g.100849195_100849204del	NCBI36
NG_053176.1:g.23357_23366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.108+169_108+178del MANE Select	ENSP00000251127.6:n.108+169_108+178del
ENST00000376200.6:c.108+169_108+178del	ENSP00000365373.5:n.108+169_108+178del
ENST00000648359.1:c.108+169_108+178del	ENSP00000497465.1:n.108+169_108+178del
ENST00000674840.1:n.206+169_206+178del
ENST00000674904.1:n.272+169_272+178del
ENST00000675150.1:c.108+169_108+178del	ENSP00000502680.1:n.108+169_108+178del
ENST00000675332.1:c.108+169_108+178del	ENSP00000501955.1:n.108+169_108+178del
ENST00000675415.1:n.291+169_291+178del
ENST00000675594.1:c.108+169_108+178del	ENSP00000502490.1:n.108+169_108+178del
ENST00000675802.1:c.108+169_108+178del	ENSP00000501818.1:n.108+169_108+178del
ENST00000676315.1:c.108+169_108+178del	ENSP00000501603.1:n.108+169_108+178del
ENST00000676357.1:n.328+169_328+178del
ENST00000676439.1:n.282+169_282+178del
ENST00000251127.10:c.108+169_108+178del	ENSP00000251127.6:n.108+169_108+178del
ENST00000376200.5:c.108+169_108+178del	ENSP00000365373.5:n.108+169_108+178del
ENST00000470333.1:n.204+169_204+178del
ENST00000497170.5:n.297+169_297+178del
NM_052867.2:c.108+169_108+178del	NP_443099.1:n.108+169_108+178del
XM_011521067.1:c.165+169_165+178del	XP_011519369.1:n.165+169_165+178del
XM_011521068.1:c.108+169_108+178del	XP_011519370.1:n.108+169_108+178del
XM_011521069.1:c.165+169_165+178del	XP_011519371.1:n.165+169_165+178del
XM_011521070.1:c.165+169_165+178del	XP_011519372.1:n.165+169_165+178del
NM_001350748.1:c.108+169_108+178del	NP_001337677.1:n.108+169_108+178del
NM_001350749.1:c.108+169_108+178del	NP_001337678.1:n.108+169_108+178del
NM_001350750.1:c.108+169_108+178del	NP_001337679.1:n.108+169_108+178del
NM_001350751.1:c.108+169_108+178del	NP_001337680.1:n.108+169_108+178del
NM_052867.3:c.108+169_108+178del	NP_443099.1:n.108+169_108+178del
XM_011521067.2:c.165+169_165+178del	XP_011519369.1:n.165+169_165+178del
XM_011521069.2:c.165+169_165+178del	XP_011519371.1:n.165+169_165+178del
XM_024449336.1:c.165+169_165+178del	XP_024305104.1:n.165+169_165+178del
NM_052867.4:c.108+169_108+178del MANE Select	NP_443099.1:n.108+169_108+178del
NM_001350748.2:c.108+169_108+178del	NP_001337677.1:n.108+169_108+178del
NM_001350749.2:c.108+169_108+178del	NP_001337678.1:n.108+169_108+178del
NM_001350750.2:c.108+169_108+178del	NP_001337679.1:n.108+169_108+178del
NM_001350751.2:c.108+169_108+178del	NP_001337680.1:n.108+169_108+178del