Canonical Allele Identifier: CA1097509588

Gene: UNCX

Linked Data

• gnomAD v3: 7-1234076-A-ACCCCCCCCCCCCCCCC
• gnomAD v4: 7-1234076-A-ACCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234085_1234086insCCCCCCCCCCCCCCCC , CM000669.2:g.1234085_1234086insCCCCCCCCCCCCCCCC	GRCh38
NC_000007.13:g.1273721_1273722insCCCCCCCCCCCCCCCC , CM000669.1:g.1273721_1273722insCCCCCCCCCCCCCCCC	GRCh37
NC_000007.12:g.1240247_1240248insCCCCCCCCCCCCCCCC	NCBI36

Transcript Alleles

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