Canonical Allele Identifier: CA413380482
Gene: UBQLN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.56591696A>C (hg19) chrX:g.56565263A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.56565263A>C , CM000685.2:g.56565263A>C GRCh38
NC_000023.10:g.56591696A>C , CM000685.1:g.56591696A>C GRCh37
NC_000023.9:g.56608421A>C NCBI36
NG_016249.1:g.6671A>C , LRG_665:g.6671A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338222.7:c.1390A>C MANE Select ENSP00000345195.5:p.Thr464Pro
ENST00000338222.6:c.1390A>C ENSP00000345195.5:p.Thr464Pro
NM_013444.3:c.1390A>C , LRG_665t1:c.1390A>C NP_038472.2:p.Thr464Pro
XM_011530837.1:c.273+1523A>C XP_011529139.1:n.273+1523A>C
NM_013444.4:c.1390A>C MANE Select NP_038472.2:p.Thr464Pro
Search 100 bp 5'
Search 100 bp 3'