Canonical Allele Identifier: CA2427845556
Gene: UBA1 HGNC NCBI

Linked Data

dbSNP Id: rs1936666212

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47206179A>C , CM000685.2:g.47206179A>C GRCh38
NC_000023.10:g.47065578A>C , CM000685.1:g.47065578A>C GRCh37
NC_000023.9:g.46950522A>C NCBI36
NG_009161.1:g.20380A>C
NG_021353.1:g.6332A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335972.11:c.1741+66A>C MANE Select ENSP00000338413.6:n.1741+66A>C
ENST00000335972.10:c.1741+66A>C ENSP00000338413.6:n.1741+66A>C
ENST00000377351.8:c.1741+66A>C ENSP00000366568.4:n.1741+66A>C
ENST00000490869.1:n.500+66A>C
NM_003334.3:c.1741+66A>C NP_003325.2:n.1741+66A>C
NM_153280.2:c.1741+66A>C NP_695012.1:n.1741+66A>C
XM_005272649.1:c.1759+66A>C XP_005272706.1:n.1759+66A>C
XM_005272650.1:c.1741+66A>C XP_005272707.1:n.1741+66A>C
XM_011543953.1:c.1825+66A>C XP_011542255.1:n.1825+66A>C
XM_011543954.1:c.1783+66A>C XP_011542256.1:n.1783+66A>C
XM_011543955.1:c.1759+66A>C XP_011542257.1:n.1759+66A>C
XM_011543956.1:c.1741+66A>C XP_011542258.1:n.1741+66A>C
XR_949047.1:n.216-829T>G
XM_011543954.2:c.1783+66A>C XP_011542256.1:n.1783+66A>C
XM_017029777.1:c.1894+66A>C XP_016885266.1:n.1894+66A>C
XM_017029778.2:c.1825+66A>C XP_016885267.1:n.1825+66A>C
XM_017029779.2:c.1759+66A>C XP_016885268.1:n.1759+66A>C
XM_017029780.1:c.1741+66A>C XP_016885269.1:n.1741+66A>C
XM_017029781.1:c.1741+66A>C XP_016885270.1:n.1741+66A>C
XR_949047.3:n.284-829T>G
NM_003334.4:c.1741+66A>C MANE Select NP_003325.2:n.1741+66A>C
NM_153280.3:c.1741+66A>C NP_695012.1:n.1741+66A>C