Canonical Allele Identifier: CA351733515
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839054T>C , CM000665.2:g.9839054T>C GRCh38
NC_000003.11:g.9880738T>C , CM000665.1:g.9880738T>C GRCh37
NC_000003.10:g.9855738T>C NCBI36
NG_054931.1:g.9965A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.818A>G (RPUSD3) MANE Select ENSP00000373331.6:p.Glu273Gly
ENST00000433535.7:c.773A>G (RPUSD3) ENSP00000398921.3:p.Glu258Gly
ENST00000383820.9:c.842A>G (RPUSD3) ENSP00000373331.5:p.Glu281Gly
ENST00000423108.5:c.328A>G (RPUSD3)
ENST00000424438.5:c.629-847A>G (RPUSD3) ENSP00000408693.1:n.629-847A>G
ENST00000427174.5:c.842A>G (RPUSD3)
ENST00000433535.6:c.797A>G (RPUSD3) ENSP00000398921.2:p.Glu266Gly
ENST00000455274.5:c.918+9659T>C (TTLL3) ENSP00000409632.1:n.918+9659T>C
ENST00000464783.1:n.801A>G (RPUSD3)
ENST00000466141.1:n.660A>G (RPUSD3)
NM_001142547.1:c.797A>G (RPUSD3) NP_001136019.1:p.Glu266Gly
NM_173659.3:c.842A>G (RPUSD3) NP_775930.2:p.Glu281Gly
XM_011533627.1:c.725-847A>G (RPUSD3) XP_011531929.1:n.725-847A>G
NM_001142547.2:c.797A>G (RPUSD3) NP_001136019.1:p.Glu266Gly
NM_001351736.1:c.629-847A>G (RPUSD3) NP_001338665.1:n.629-847A>G
NM_001351737.1:c.725-847A>G (RPUSD3) NP_001338666.1:n.725-847A>G
NM_001351738.1:c.870A>G (RPUSD3) NP_001338667.1:p.Ter290Trp
NM_173659.4:c.842A>G (RPUSD3) NP_775930.2:p.Glu281Gly
XM_024453471.1:c.842A>G (RPUSD3) XP_024309239.1:p.Glu281Gly
XM_024453472.1:c.724+1130A>G (RPUSD3) XP_024309240.1:n.724+1130A>G
NM_001351736.2:c.629-847A>G (RPUSD3) NP_001338665.1:n.629-847A>G
NM_001351736.3:c.629-847A>G (RPUSD3) NP_001338665.1:n.629-847A>G
NM_001142547.3:c.773A>G (RPUSD3) NP_001136019.2:p.Glu258Gly
NM_001351737.2:c.701-847A>G (RPUSD3) NP_001338666.2:n.701-847A>G
NM_001351738.2:c.846A>G (RPUSD3) NP_001338667.2:p.Ter282Trp
NM_173659.5:c.818A>G (RPUSD3) MANE Select NP_775930.3:p.Glu273Gly