Canonical Allele Identifier: CA2527815066

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234085_1234086insCCCCCCCCCCCCCCCCCCACC , CM000669.2:g.1234085_1234086insCCCCCCCCCCCCCCCCCCACC	GRCh38
NC_000007.13:g.1273721_1273722insCCCCCCCCCCCCCCCCCCACC , CM000669.1:g.1273721_1273722insCCCCCCCCCCCCCCCCCCACC	GRCh37
NC_000007.12:g.1240247_1240248insCCCCCCCCCCCCCCCCCCACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+390_450+391insCCCCCCCCCCCCCCCCCCACC MANE Select	ENSP00000314480.8:n.450+390_450+391insCCCCCCCCCCCCCCCCCCACC
ENST00000316333.8:c.450+390_450+391insCCCCCCCCCCCCCCCCCCACC	ENSP00000314480.8:n.450+390_450+391insCCCCCCCCCCCCCCCCCCACC
NM_001080461.1:c.450+390_450+391insCCCCCCCCCCCCCCCCCCACC	NP_001073930.1:n.450+390_450+391insCCCCCCCCCCCCCCCCCCACC
NM_001080461.2:c.450+390_450+391insCCCCCCCCCCCCCCCCCCACC	NP_001073930.1:n.450+390_450+391insCCCCCCCCCCCCCCCCCCACC
NM_001080461.3:c.450+390_450+391insCCCCCCCCCCCCCCCCCCACC MANE Select	NP_001073930.1:n.450+390_450+391insCCCCCCCCCCCCCCCCCCACC