Canonical Allele Identifier: CA351733376
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839037T>A , CM000665.2:g.9839037T>A GRCh38
NC_000003.11:g.9880721T>A , CM000665.1:g.9880721T>A GRCh37
NC_000003.10:g.9855721T>A NCBI36
NG_054931.1:g.9982A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.835A>T (RPUSD3) MANE Select ENSP00000373331.6:p.Arg279Ter
ENST00000433535.7:c.790A>T (RPUSD3) ENSP00000398921.3:p.Arg264Ter
ENST00000383820.9:c.859A>T (RPUSD3) ENSP00000373331.5:p.Arg287Ter
ENST00000423108.5:c.345A>T (RPUSD3)
ENST00000424438.5:c.629-830A>T (RPUSD3) ENSP00000408693.1:n.629-830A>T
ENST00000427174.5:c.859A>T (RPUSD3)
ENST00000433535.6:c.814A>T (RPUSD3) ENSP00000398921.2:p.Arg272Ter
ENST00000455274.5:c.918+9642T>A (TTLL3) ENSP00000409632.1:n.918+9642T>A
ENST00000464783.1:n.818A>T (RPUSD3)
ENST00000466141.1:n.677A>T (RPUSD3)
NM_001142547.1:c.814A>T (RPUSD3) NP_001136019.1:p.Arg272Ter
NM_173659.3:c.859A>T (RPUSD3) NP_775930.2:p.Arg287Ter
XM_011533627.1:c.725-830A>T (RPUSD3) XP_011531929.1:n.725-830A>T
NM_001142547.2:c.814A>T (RPUSD3) NP_001136019.1:p.Arg272Ter
NM_001351736.1:c.629-830A>T (RPUSD3) NP_001338665.1:n.629-830A>T
NM_001351737.1:c.725-830A>T (RPUSD3) NP_001338666.1:n.725-830A>T
NM_001351738.1:c.*17A>T (RPUSD3) NP_001338667.1:n.*17A>T
NM_173659.4:c.859A>T (RPUSD3) NP_775930.2:p.Arg287Ter
XM_024453471.1:c.859A>T (RPUSD3) XP_024309239.1:p.Arg287Ter
XM_024453472.1:c.724+1147A>T (RPUSD3) XP_024309240.1:n.724+1147A>T
NM_001351736.2:c.629-830A>T (RPUSD3) NP_001338665.1:n.629-830A>T
NM_001351736.3:c.629-830A>T (RPUSD3) NP_001338665.1:n.629-830A>T
NM_001142547.3:c.790A>T (RPUSD3) NP_001136019.2:p.Arg264Ter
NM_001351737.2:c.701-830A>T (RPUSD3) NP_001338666.2:n.701-830A>T
NM_001351738.2:c.*17A>T (RPUSD3) NP_001338667.2:n.*17A>T
NM_173659.5:c.835A>T (RPUSD3) MANE Select NP_775930.3:p.Arg279Ter