Canonical Allele Identifier: CA1682451607

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234134_1234142delinsGGAGCGAAC , CM000669.2:g.1234134_1234142delinsGGAGCGAAC	GRCh38
NC_000007.13:g.1273770_1273778delinsGGAGCGAAC , CM000669.1:g.1273770_1273778delinsGGAGCGAAC	GRCh37
NC_000007.12:g.1240296_1240304delinsGGAGCGAAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+439_450+447delinsGGAGCGAAC MANE Select	ENSP00000314480.8:n.450+439_450+447delinsGGAGCGAAC
ENST00000316333.8:c.450+439_450+447delinsGGAGCGAAC	ENSP00000314480.8:n.450+439_450+447delinsGGAGCGAAC
NM_001080461.1:c.450+439_450+447delinsGGAGCGAAC	NP_001073930.1:n.450+439_450+447delinsGGAGCGAAC
NM_001080461.2:c.450+439_450+447delinsGGAGCGAAC	NP_001073930.1:n.450+439_450+447delinsGGAGCGAAC
NM_001080461.3:c.450+439_450+447delinsGGAGCGAAC MANE Select	NP_001073930.1:n.450+439_450+447delinsGGAGCGAAC