Canonical Allele Identifier: CA832638579
Gene: UNCX HGNC NCBI

Linked Data

dbSNP Id: rs1440841259
gnomAD v3: 7-1234134-GGAGCGAAC-G
gnomAD v4: 7-1234134-GGAGCGAAC-G
MyVariant Identifiers: chr7:g.1273771_1273778del (hg19) chr7:g.1234135_1234142del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234138_1234145del , CM000669.2:g.1234138_1234145del GRCh38
NC_000007.13:g.1273774_1273781del , CM000669.1:g.1273774_1273781del GRCh37
NC_000007.12:g.1240300_1240307del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316333.9:c.450+443_450+450del MANE Select ENSP00000314480.8:n.450+443_450+450del
ENST00000316333.8:c.450+443_450+450del ENSP00000314480.8:n.450+443_450+450del
NM_001080461.1:c.450+443_450+450del NP_001073930.1:n.450+443_450+450del
NM_001080461.2:c.450+443_450+450del NP_001073930.1:n.450+443_450+450del
NM_001080461.3:c.450+443_450+450del MANE Select NP_001073930.1:n.450+443_450+450del
Search 100 bp 5'
Search 100 bp 3'