Canonical Allele Identifier: CA2579594783
Gene: UBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47206137_47206139del , CM000685.2:g.47206137_47206139del GRCh38
NC_000023.10:g.47065536_47065538del , CM000685.1:g.47065536_47065538del GRCh37
NC_000023.9:g.46950480_46950482del NCBI36
NG_009161.1:g.20338_20340del
NG_021353.1:g.6290_6292del

Transcript Alleles

HGVS Amino-acid Change
ENST00000335972.11:c.1741+24_1741+26del MANE Select ENSP00000338413.6:n.1741+24_1741+26del
ENST00000335972.10:c.1741+24_1741+26del ENSP00000338413.6:n.1741+24_1741+26del
ENST00000377351.8:c.1741+24_1741+26del ENSP00000366568.4:n.1741+24_1741+26del
ENST00000490869.1:n.500+24_500+26del
NM_003334.3:c.1741+24_1741+26del NP_003325.2:n.1741+24_1741+26del
NM_153280.2:c.1741+24_1741+26del NP_695012.1:n.1741+24_1741+26del
XM_005272649.1:c.1759+24_1759+26del XP_005272706.1:n.1759+24_1759+26del
XM_005272650.1:c.1741+24_1741+26del XP_005272707.1:n.1741+24_1741+26del
XM_011543953.1:c.1825+24_1825+26del XP_011542255.1:n.1825+24_1825+26del
XM_011543954.1:c.1783+24_1783+26del XP_011542256.1:n.1783+24_1783+26del
XM_011543955.1:c.1759+24_1759+26del XP_011542257.1:n.1759+24_1759+26del
XM_011543956.1:c.1741+24_1741+26del XP_011542258.1:n.1741+24_1741+26del
XR_949047.1:n.216-786_216-784del
XM_011543954.2:c.1783+24_1783+26del XP_011542256.1:n.1783+24_1783+26del
XM_017029777.1:c.1894+24_1894+26del XP_016885266.1:n.1894+24_1894+26del
XM_017029778.2:c.1825+24_1825+26del XP_016885267.1:n.1825+24_1825+26del
XM_017029779.2:c.1759+24_1759+26del XP_016885268.1:n.1759+24_1759+26del
XM_017029780.1:c.1741+24_1741+26del XP_016885269.1:n.1741+24_1741+26del
XM_017029781.1:c.1741+24_1741+26del XP_016885270.1:n.1741+24_1741+26del
XR_949047.3:n.284-786_284-784del
NM_003334.4:c.1741+24_1741+26del MANE Select NP_003325.2:n.1741+24_1741+26del
NM_153280.3:c.1741+24_1741+26del NP_695012.1:n.1741+24_1741+26del