Canonical Allele Identifier: CA412802214

Gene: UBA1

Linked Data

• MyVariant Identifiers: chrX:g.47065504T>G (hg19) ; chrX:g.47206105T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47206105T>G , CM000685.2:g.47206105T>G	GRCh38
NC_000023.10:g.47065504T>G , CM000685.1:g.47065504T>G	GRCh37
NC_000023.9:g.46950448T>G	NCBI36
NG_009161.1:g.20306T>G
NG_021353.1:g.6258T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000335972.11:c.1733T>G MANE Select	ENSP00000338413.6:p.Val578Gly
ENST00000335972.10:c.1733T>G	ENSP00000338413.6:p.Val578Gly
ENST00000377351.8:c.1733T>G	ENSP00000366568.4:p.Val578Gly
ENST00000490869.1:n.492T>G
NM_003334.3:c.1733T>G	NP_003325.2:p.Val578Gly
NM_153280.2:c.1733T>G	NP_695012.1:p.Val578Gly
XM_005272649.1:c.1751T>G	XP_005272706.1:p.Val584Gly
XM_005272650.1:c.1733T>G	XP_005272707.1:p.Val578Gly
XM_011543953.1:c.1817T>G	XP_011542255.1:p.Val606Gly
XM_011543954.1:c.1775T>G	XP_011542256.1:p.Val592Gly
XM_011543955.1:c.1751T>G	XP_011542257.1:p.Val584Gly
XM_011543956.1:c.1733T>G	XP_011542258.1:p.Val578Gly
XR_949047.1:n.216-755A>C
XM_011543954.2:c.1775T>G	XP_011542256.1:p.Val592Gly
XM_017029777.1:c.1886T>G	XP_016885266.1:p.Val629Gly
XM_017029778.2:c.1817T>G	XP_016885267.1:p.Val606Gly
XM_017029779.2:c.1751T>G	XP_016885268.1:p.Val584Gly
XM_017029780.1:c.1733T>G	XP_016885269.1:p.Val578Gly
XM_017029781.1:c.1733T>G	XP_016885270.1:p.Val578Gly
XR_949047.3:n.284-755A>C
NM_003334.4:c.1733T>G MANE Select	NP_003325.2:p.Val578Gly
NM_153280.3:c.1733T>G	NP_695012.1:p.Val578Gly