Canonical Allele Identifier: CA351733458
Gene: RPUSD3 HGNC NCBI
TTLL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9839047G>C , CM000665.2:g.9839047G>C GRCh38
NC_000003.11:g.9880731G>C , CM000665.1:g.9880731G>C GRCh37
NC_000003.10:g.9855731G>C NCBI36
NG_054931.1:g.9972C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000383820.10:c.825C>G (RPUSD3) MANE Select ENSP00000373331.6:p.Asn275Lys
ENST00000433535.7:c.780C>G (RPUSD3) ENSP00000398921.3:p.Asn260Lys
ENST00000383820.9:c.849C>G (RPUSD3) ENSP00000373331.5:p.Asn283Lys
ENST00000423108.5:c.335C>G (RPUSD3)
ENST00000424438.5:c.629-840C>G (RPUSD3) ENSP00000408693.1:n.629-840C>G
ENST00000427174.5:c.849C>G (RPUSD3)
ENST00000433535.6:c.804C>G (RPUSD3) ENSP00000398921.2:p.Asn268Lys
ENST00000455274.5:c.918+9652G>C (TTLL3) ENSP00000409632.1:n.918+9652G>C
ENST00000464783.1:n.808C>G (RPUSD3)
ENST00000466141.1:n.667C>G (RPUSD3)
NM_001142547.1:c.804C>G (RPUSD3) NP_001136019.1:p.Asn268Lys
NM_173659.3:c.849C>G (RPUSD3) NP_775930.2:p.Asn283Lys
XM_011533627.1:c.725-840C>G (RPUSD3) XP_011531929.1:n.725-840C>G
NM_001142547.2:c.804C>G (RPUSD3) NP_001136019.1:p.Asn268Lys
NM_001351736.1:c.629-840C>G (RPUSD3) NP_001338665.1:n.629-840C>G
NM_001351737.1:c.725-840C>G (RPUSD3) NP_001338666.1:n.725-840C>G
NM_001351738.1:c.*7C>G (RPUSD3) NP_001338667.1:n.*7C>G
NM_173659.4:c.849C>G (RPUSD3) NP_775930.2:p.Asn283Lys
XM_024453471.1:c.849C>G (RPUSD3) XP_024309239.1:p.Asn283Lys
XM_024453472.1:c.724+1137C>G (RPUSD3) XP_024309240.1:n.724+1137C>G
NM_001351736.2:c.629-840C>G (RPUSD3) NP_001338665.1:n.629-840C>G
NM_001351736.3:c.629-840C>G (RPUSD3) NP_001338665.1:n.629-840C>G
NM_001142547.3:c.780C>G (RPUSD3) NP_001136019.2:p.Asn260Lys
NM_001351737.2:c.701-840C>G (RPUSD3) NP_001338666.2:n.701-840C>G
NM_001351738.2:c.*7C>G (RPUSD3) NP_001338667.2:n.*7C>G
NM_173659.5:c.825C>G (RPUSD3) MANE Select NP_775930.3:p.Asn275Lys