Canonical Allele Identifier: CA1671754675
Gene: UST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.148949693G= , CM000668.2:g.148949693G= GRCh38
NC_000006.11:g.149270829G= , CM000668.1:g.149270829G= GRCh37
NC_000006.10:g.149312522G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367463.5:c.448-4179G= MANE Select ENSP00000356433.4:n.448-4179G=
ENST00000367463.4:c.448-4179G= ENSP00000356433.4:n.448-4179G=
NM_005715.2:c.448-4179G= NP_005706.1:n.448-4179G=
XM_005266790.3:c.448-4179G= XP_005266847.1:n.448-4179G=
XM_011535376.1:c.448-4179G= XP_011533678.1:n.448-4179G=
XM_011535377.1:c.448-4179G= XP_011533679.1:n.448-4179G=
XM_011535378.1:c.448-4179G= XP_011533680.1:n.448-4179G=
XR_942249.1:n.917-4179G=
XM_011535378.3:c.448-4179G= XP_011533680.1:n.448-4179G=
XM_017010152.1:c.448-4179G= XP_016865641.1:n.448-4179G=
XR_001743088.2:n.452-4179G=
NM_005715.3:c.448-4179G= MANE Select NP_005706.1:n.448-4179G=