Canonical Allele Identifier: CA516701407
Gene: UBQLN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.56591698A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.56565265A>G , CM000685.2:g.56565265A>G GRCh38
NC_000023.10:g.56591698A>G , CM000685.1:g.56591698A>G GRCh37
NC_000023.9:g.56608423A>G NCBI36
NG_016249.1:g.6673A>G , LRG_665:g.6673A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338222.7:c.1392A>G MANE Select ENSP00000345195.5:p.Thr464=
ENST00000338222.6:c.1392A>G ENSP00000345195.5:p.Thr464=
NM_013444.3:c.1392A>G , LRG_665t1:c.1392A>G NP_038472.2:p.Thr464=
XM_011530837.1:c.273+1525A>G XP_011529139.1:n.273+1525A>G
NM_013444.4:c.1392A>G MANE Select NP_038472.2:p.Thr464=
Search 100 bp 5'
Search 100 bp 3'