Canonical Allele Identifier: CA351733736
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839088T>G , CM000665.2:g.9839088T>G GRCh38
NC_000003.11:g.9880772T>G , CM000665.1:g.9880772T>G GRCh37
NC_000003.10:g.9855772T>G NCBI36
NG_054931.1:g.9931A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.784A>C (RPUSD3) MANE Select ENSP00000373331.6:p.Thr262Pro
ENST00000433535.7:c.739A>C (RPUSD3) ENSP00000398921.3:p.Thr247Pro
ENST00000383820.9:c.808A>C (RPUSD3) ENSP00000373331.5:p.Thr270Pro
ENST00000423108.5:c.294A>C (RPUSD3)
ENST00000424438.5:c.629-881A>C (RPUSD3) ENSP00000408693.1:n.629-881A>C
ENST00000427174.5:c.808A>C (RPUSD3)
ENST00000433535.6:c.763A>C (RPUSD3) ENSP00000398921.2:p.Thr255Pro
ENST00000455274.5:c.918+9693T>G (TTLL3) ENSP00000409632.1:n.918+9693T>G
ENST00000464783.1:n.767A>C (RPUSD3)
ENST00000466141.1:n.626A>C (RPUSD3)
NM_001142547.1:c.763A>C (RPUSD3) NP_001136019.1:p.Thr255Pro
NM_173659.3:c.808A>C (RPUSD3) NP_775930.2:p.Thr270Pro
XM_011533627.1:c.725-881A>C (RPUSD3) XP_011531929.1:n.725-881A>C
NM_001142547.2:c.763A>C (RPUSD3) NP_001136019.1:p.Thr255Pro
NM_001351736.1:c.629-881A>C (RPUSD3) NP_001338665.1:n.629-881A>C
NM_001351737.1:c.725-881A>C (RPUSD3) NP_001338666.1:n.725-881A>C
NM_001351738.1:c.836A>C (RPUSD3) NP_001338667.1:p.His279Pro
NM_173659.4:c.808A>C (RPUSD3) NP_775930.2:p.Thr270Pro
XM_024453471.1:c.808A>C (RPUSD3) XP_024309239.1:p.Thr270Pro
XM_024453472.1:c.724+1096A>C (RPUSD3) XP_024309240.1:n.724+1096A>C
NM_001351736.2:c.629-881A>C (RPUSD3) NP_001338665.1:n.629-881A>C
NM_001351736.3:c.629-881A>C (RPUSD3) NP_001338665.1:n.629-881A>C
NM_001142547.3:c.739A>C (RPUSD3) NP_001136019.2:p.Thr247Pro
NM_001351737.2:c.701-881A>C (RPUSD3) NP_001338666.2:n.701-881A>C
NM_001351738.2:c.812A>C (RPUSD3) NP_001338667.2:p.His271Pro
NM_173659.5:c.784A>C (RPUSD3) MANE Select NP_775930.3:p.Thr262Pro