Canonical Allele Identifier: CA516351799
Gene: UBA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.47065451T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47206052T>C , CM000685.2:g.47206052T>C GRCh38
NC_000023.10:g.47065451T>C , CM000685.1:g.47065451T>C GRCh37
NC_000023.9:g.46950395T>C NCBI36
NG_009161.1:g.20253T>C
NG_021353.1:g.6205T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000335972.11:c.1680T>C MANE Select ENSP00000338413.6:p.Tyr560=
ENST00000335972.10:c.1680T>C ENSP00000338413.6:p.Tyr560=
ENST00000377351.8:c.1680T>C ENSP00000366568.4:p.Tyr560=
ENST00000490869.1:n.465-26T>C
NM_003334.3:c.1680T>C NP_003325.2:p.Tyr560=
NM_153280.2:c.1680T>C NP_695012.1:p.Tyr560=
XM_005272649.1:c.1698T>C XP_005272706.1:p.Tyr566=
XM_005272650.1:c.1680T>C XP_005272707.1:p.Tyr560=
XM_011543953.1:c.1764T>C XP_011542255.1:p.Tyr588=
XM_011543954.1:c.1722T>C XP_011542256.1:p.Tyr574=
XM_011543955.1:c.1698T>C XP_011542257.1:p.Tyr566=
XM_011543956.1:c.1680T>C XP_011542258.1:p.Tyr560=
XR_949047.1:n.216-702A>G
XM_011543954.2:c.1722T>C XP_011542256.1:p.Tyr574=
XM_017029777.1:c.1833T>C XP_016885266.1:p.Tyr611=
XM_017029778.2:c.1764T>C XP_016885267.1:p.Tyr588=
XM_017029779.2:c.1698T>C XP_016885268.1:p.Tyr566=
XM_017029780.1:c.1680T>C XP_016885269.1:p.Tyr560=
XM_017029781.1:c.1680T>C XP_016885270.1:p.Tyr560=
XR_949047.3:n.284-702A>G
NM_003334.4:c.1680T>C MANE Select NP_003325.2:p.Tyr560=
NM_153280.3:c.1680T>C NP_695012.1:p.Tyr560=