Canonical Allele Identifier: CA2573051560

Gene: NCDN

Linked Data

• ClinVar Variation Id: 1320191
• ClinVar RCV Id: RCV001775364
• dbSNP Id: rs2148538021

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.35561141dup , CM000663.2:g.35561141dup	GRCh38
NC_000001.10:g.36026742dup , CM000663.1:g.36026742dup	GRCh37
NC_000001.9:g.35799329dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373243.7:c.990dup MANE Select	ENSP00000362340.2:p.Glu331ArgfsTer22
ENST00000356090.8:c.990dup	ENSP00000348394.4:p.Glu331ArgfsTer22
ENST00000373243.6:c.990dup	ENSP00000362340.2:p.Glu331ArgfsTer22
ENST00000373253.7:c.939dup	ENSP00000362350.3:p.Glu314ArgfsTer22
NM_001014839.1:c.990dup	NP_001014839.1:p.Glu331ArgfsTer22
NM_001014841.1:c.939dup	NP_001014841.1:p.Glu314ArgfsTer22
NM_014284.2:c.990dup	NP_055099.1:p.Glu331ArgfsTer22
NM_014284.3:c.990dup MANE Select	NP_055099.1:p.Glu331ArgfsTer22
NM_001014839.2:c.990dup	NP_001014839.1:p.Glu331ArgfsTer22
NM_001014841.2:c.939dup	NP_001014841.1:p.Glu314ArgfsTer22