Canonical Allele Identifier: CA412801439
Gene: UBA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.47206014C>A , CM000685.2:g.47206014C>A GRCh38
NC_000023.10:g.47065413C>A , CM000685.1:g.47065413C>A GRCh37
NC_000023.9:g.46950357C>A NCBI36
NG_009161.1:g.20215C>A
NG_021353.1:g.6167C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335972.11:c.1642C>A MANE Select ENSP00000338413.6:p.His548Asn
ENST00000335972.10:c.1642C>A ENSP00000338413.6:p.His548Asn
ENST00000377351.8:c.1642C>A ENSP00000366568.4:p.His548Asn
ENST00000490869.1:n.465-64C>A
NM_003334.3:c.1642C>A NP_003325.2:p.His548Asn
NM_153280.2:c.1642C>A NP_695012.1:p.His548Asn
XM_005272649.1:c.1660C>A XP_005272706.1:p.His554Asn
XM_005272650.1:c.1642C>A XP_005272707.1:p.His548Asn
XM_011543953.1:c.1726C>A XP_011542255.1:p.His576Asn
XM_011543954.1:c.1684C>A XP_011542256.1:p.His562Asn
XM_011543955.1:c.1660C>A XP_011542257.1:p.His554Asn
XM_011543956.1:c.1642C>A XP_011542258.1:p.His548Asn
XR_949047.1:n.216-664G>T
XM_011543954.2:c.1684C>A XP_011542256.1:p.His562Asn
XM_017029777.1:c.1795C>A XP_016885266.1:p.His599Asn
XM_017029778.2:c.1726C>A XP_016885267.1:p.His576Asn
XM_017029779.2:c.1660C>A XP_016885268.1:p.His554Asn
XM_017029780.1:c.1642C>A XP_016885269.1:p.His548Asn
XM_017029781.1:c.1642C>A XP_016885270.1:p.His548Asn
XR_949047.3:n.284-664G>T
NM_003334.4:c.1642C>A MANE Select NP_003325.2:p.His548Asn
NM_153280.3:c.1642C>A NP_695012.1:p.His548Asn