Canonical Allele Identifier: CA1344929531
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839013_9839016delinsGGCA , CM000665.2:g.9839013_9839016delinsGGCA GRCh38
NC_000003.11:g.9880697_9880700delinsGGCA , CM000665.1:g.9880697_9880700delinsGGCA GRCh37
NC_000003.10:g.9855697_9855700delinsGGCA NCBI36
NG_054931.1:g.10003_10006delinsTGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.840+16_840+19delinsTGCC (RPUSD3) MANE Select ENSP00000373331.6:n.840+16_840+19delinsTGCC
ENST00000433535.7:c.795+16_795+19delinsTGCC (RPUSD3) ENSP00000398921.3:n.795+16_795+19delinsTGCC
ENST00000383820.9:c.864+16_864+19delinsTGCC (RPUSD3) ENSP00000373331.5:n.864+16_864+19delinsTGCC
ENST00000423108.5:c.366_369delinsTGCC (RPUSD3)
ENST00000424438.5:c.629-809_629-806delinsTGCC (RPUSD3) ENSP00000408693.1:n.629-809_629-806delinsTGCC
ENST00000427174.5:c.864+16_864+19delinsTGCC (RPUSD3)
ENST00000433535.6:c.819+16_819+19delinsTGCC (RPUSD3) ENSP00000398921.2:n.819+16_819+19delinsTGCC
ENST00000455274.5:c.918+9618_918+9621delinsGGCA (TTLL3) ENSP00000409632.1:n.918+9618_918+9621delinsGGCA
ENST00000464783.1:n.823+16_823+19delinsTGCC (RPUSD3)
ENST00000466141.1:n.682+16_682+19delinsTGCC (RPUSD3)
NM_001142547.1:c.819+16_819+19delinsTGCC (RPUSD3) NP_001136019.1:n.819+16_819+19delinsTGCC
NM_173659.3:c.864+16_864+19delinsTGCC (RPUSD3) NP_775930.2:n.864+16_864+19delinsTGCC
XM_011533627.1:c.725-809_725-806delinsTGCC (RPUSD3) XP_011531929.1:n.725-809_725-806delinsTGCC
NM_001142547.2:c.819+16_819+19delinsTGCC (RPUSD3) NP_001136019.1:n.819+16_819+19delinsTGCC
NM_001351736.1:c.629-809_629-806delinsTGCC (RPUSD3) NP_001338665.1:n.629-809_629-806delinsTGCC
NM_001351737.1:c.725-809_725-806delinsTGCC (RPUSD3) NP_001338666.1:n.725-809_725-806delinsTGCC
NM_001351738.1:c.*22+16_*22+19delinsTGCC (RPUSD3) NP_001338667.1:n.*22+16_*22+19delinsTGCC
NM_173659.4:c.864+16_864+19delinsTGCC (RPUSD3) NP_775930.2:n.864+16_864+19delinsTGCC
XM_024453471.1:c.880_883delinsTGCC (RPUSD3) XP_024309239.1:p.Cys294=
XM_024453472.1:c.724+1168_724+1171delinsTGCC (RPUSD3) XP_024309240.1:n.724+1168_724+1171delinsTGCC
NM_001351736.2:c.629-809_629-806delinsTGCC (RPUSD3) NP_001338665.1:n.629-809_629-806delinsTGCC
NM_001351736.3:c.629-809_629-806delinsTGCC (RPUSD3) NP_001338665.1:n.629-809_629-806delinsTGCC
NM_001142547.3:c.795+16_795+19delinsTGCC (RPUSD3) NP_001136019.2:n.795+16_795+19delinsTGCC
NM_001351737.2:c.701-809_701-806delinsTGCC (RPUSD3) NP_001338666.2:n.701-809_701-806delinsTGCC
NM_001351738.2:c.*22+16_*22+19delinsTGCC (RPUSD3) NP_001338667.2:n.*22+16_*22+19delinsTGCC
NM_173659.5:c.840+16_840+19delinsTGCC (RPUSD3) MANE Select NP_775930.3:n.840+16_840+19delinsTGCC