Canonical Allele Identifier: CA351734040
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839117C>T , CM000665.2:g.9839117C>T GRCh38
NC_000003.11:g.9880801C>T , CM000665.1:g.9880801C>T GRCh37
NC_000003.10:g.9855801C>T NCBI36
NG_054931.1:g.9902G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.755G>A (RPUSD3) MANE Select ENSP00000373331.6:p.Gly252Glu
ENST00000433535.7:c.710G>A (RPUSD3) ENSP00000398921.3:p.Gly237Glu
ENST00000383820.9:c.779G>A (RPUSD3) ENSP00000373331.5:p.Gly260Glu
ENST00000423108.5:c.265G>A (RPUSD3)
ENST00000424438.5:c.629-910G>A (RPUSD3) ENSP00000408693.1:n.629-910G>A
ENST00000427174.5:c.779G>A (RPUSD3)
ENST00000433535.6:c.734G>A (RPUSD3) ENSP00000398921.2:p.Gly245Glu
ENST00000455274.5:c.918+9722C>T (TTLL3) ENSP00000409632.1:n.918+9722C>T
ENST00000464783.1:n.738G>A (RPUSD3)
ENST00000466141.1:n.597G>A (RPUSD3)
NM_001142547.1:c.734G>A (RPUSD3) NP_001136019.1:p.Gly245Glu
NM_173659.3:c.779G>A (RPUSD3) NP_775930.2:p.Gly260Glu
XM_011533627.1:c.725-910G>A (RPUSD3) XP_011531929.1:n.725-910G>A
NM_001142547.2:c.734G>A (RPUSD3) NP_001136019.1:p.Gly245Glu
NM_001351736.1:c.629-910G>A (RPUSD3) NP_001338665.1:n.629-910G>A
NM_001351737.1:c.725-910G>A (RPUSD3) NP_001338666.1:n.725-910G>A
NM_001351738.1:c.807G>A (RPUSD3) NP_001338667.1:p.Trp269Ter
NM_173659.4:c.779G>A (RPUSD3) NP_775930.2:p.Gly260Glu
XM_024453471.1:c.779G>A (RPUSD3) XP_024309239.1:p.Gly260Glu
XM_024453472.1:c.724+1067G>A (RPUSD3) XP_024309240.1:n.724+1067G>A
NM_001351736.2:c.629-910G>A (RPUSD3) NP_001338665.1:n.629-910G>A
NM_001351736.3:c.629-910G>A (RPUSD3) NP_001338665.1:n.629-910G>A
NM_001142547.3:c.710G>A (RPUSD3) NP_001136019.2:p.Gly237Glu
NM_001351737.2:c.701-910G>A (RPUSD3) NP_001338666.2:n.701-910G>A
NM_001351738.2:c.783G>A (RPUSD3) NP_001338667.2:p.Trp261Ter
NM_173659.5:c.755G>A (RPUSD3) MANE Select NP_775930.3:p.Gly252Glu