Canonical Allele Identifier: CA572109210
Gene: UNCX HGNC NCBI

Linked Data

gnomAD v2: 7-1273741-CTT-C
gnomAD v3: 7-1234105-CTT-C
gnomAD v4: 7-1234105-CTT-C
MyVariant Identifiers: chr7:g.1273742_1273743del (hg19) chr7:g.1234106_1234107del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.1234106_1234107del , CM000669.2:g.1234106_1234107del GRCh38
NC_000007.13:g.1273742_1273743del , CM000669.1:g.1273742_1273743del GRCh37
NC_000007.12:g.1240268_1240269del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000316333.9:c.450+411_450+412del MANE Select ENSP00000314480.8:n.450+411_450+412del
ENST00000316333.8:c.450+411_450+412del ENSP00000314480.8:n.450+411_450+412del
NM_001080461.1:c.450+411_450+412del NP_001073930.1:n.450+411_450+412del
NM_001080461.2:c.450+411_450+412del NP_001073930.1:n.450+411_450+412del
NM_001080461.3:c.450+411_450+412del MANE Select NP_001073930.1:n.450+411_450+412del
Search 100 bp 5'
Search 100 bp 3'