Canonical Allele Identifier: CA351734388
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839161A>T , CM000665.2:g.9839161A>T GRCh38
NC_000003.11:g.9880845A>T , CM000665.1:g.9880845A>T GRCh37
NC_000003.10:g.9855845A>T NCBI36
NG_054931.1:g.9858T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000383820.10:c.711T>A (RPUSD3) MANE Select ENSP00000373331.6:p.Ser237Arg
ENST00000433535.7:c.666T>A (RPUSD3) ENSP00000398921.3:p.Ser222Arg
ENST00000383820.9:c.735T>A (RPUSD3) ENSP00000373331.5:p.Ser245Arg
ENST00000423108.5:c.221T>A (RPUSD3)
ENST00000424438.5:c.629-954T>A (RPUSD3) ENSP00000408693.1:n.629-954T>A
ENST00000427174.5:c.735T>A (RPUSD3)
ENST00000433535.6:c.690T>A (RPUSD3) ENSP00000398921.2:p.Ser230Arg
ENST00000455274.5:c.918+9766A>T (TTLL3) ENSP00000409632.1:n.918+9766A>T
ENST00000464783.1:n.694T>A (RPUSD3)
ENST00000466141.1:n.553T>A (RPUSD3)
NM_001142547.1:c.690T>A (RPUSD3) NP_001136019.1:p.Ser230Arg
NM_173659.3:c.735T>A (RPUSD3) NP_775930.2:p.Ser245Arg
XM_011533627.1:c.725-954T>A (RPUSD3) XP_011531929.1:n.725-954T>A
NM_001142547.2:c.690T>A (RPUSD3) NP_001136019.1:p.Ser230Arg
NM_001351736.1:c.629-954T>A (RPUSD3) NP_001338665.1:n.629-954T>A
NM_001351737.1:c.725-954T>A (RPUSD3) NP_001338666.1:n.725-954T>A
NM_001351738.1:c.763T>A (RPUSD3) NP_001338667.1:p.Ser255Thr
NM_173659.4:c.735T>A (RPUSD3) NP_775930.2:p.Ser245Arg
XM_024453471.1:c.735T>A (RPUSD3) XP_024309239.1:p.Ser245Arg
XM_024453472.1:c.724+1023T>A (RPUSD3) XP_024309240.1:n.724+1023T>A
NM_001351736.2:c.629-954T>A (RPUSD3) NP_001338665.1:n.629-954T>A
NM_001351736.3:c.629-954T>A (RPUSD3) NP_001338665.1:n.629-954T>A
NM_001142547.3:c.666T>A (RPUSD3) NP_001136019.2:p.Ser222Arg
NM_001351737.2:c.701-954T>A (RPUSD3) NP_001338666.2:n.701-954T>A
NM_001351738.2:c.739T>A (RPUSD3) NP_001338667.2:p.Ser247Thr
NM_173659.5:c.711T>A (RPUSD3) MANE Select NP_775930.3:p.Ser237Arg