Canonical Allele Identifier: CA339346070

Gene: NCDN

Linked Data

• ClinVar Variation Id: 2323585
• ClinVar RCV Id: RCV004164981
• MyVariant Identifiers: chr1:g.36028204C>G (hg19) ; chr1:g.35562603C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.35562603C>G , CM000663.2:g.35562603C>G	GRCh38
NC_000001.10:g.36028204C>G , CM000663.1:g.36028204C>G	GRCh37
NC_000001.9:g.35800791C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373243.7:c.1355C>G MANE Select	ENSP00000362340.2:p.Pro452Arg
ENST00000356090.8:c.1355C>G	ENSP00000348394.4:p.Pro452Arg
ENST00000373243.6:c.1355C>G	ENSP00000362340.2:p.Pro452Arg
ENST00000373253.7:c.1304C>G	ENSP00000362350.3:p.Pro435Arg
ENST00000423723.1:c.136C>G
NM_001014839.1:c.1355C>G	NP_001014839.1:p.Pro452Arg
NM_001014841.1:c.1304C>G	NP_001014841.1:p.Pro435Arg
NM_014284.2:c.1355C>G	NP_055099.1:p.Pro452Arg
NM_014284.3:c.1355C>G MANE Select	NP_055099.1:p.Pro452Arg
NM_001014839.2:c.1355C>G	NP_001014839.1:p.Pro452Arg
NM_001014841.2:c.1304C>G	NP_001014841.1:p.Pro435Arg