Canonical Allele Identifier: CA1344929460

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9838943_9838967delinsCAAGCTGCACAGATAAGGTCTGGAG , CM000665.2:g.9838943_9838967delinsCAAGCTGCACAGATAAGGTCTGGAG	GRCh38
NC_000003.11:g.9880627_9880651delinsCAAGCTGCACAGATAAGGTCTGGAG , CM000665.1:g.9880627_9880651delinsCAAGCTGCACAGATAAGGTCTGGAG	GRCh37
NC_000003.10:g.9855627_9855651delinsCAAGCTGCACAGATAAGGTCTGGAG	NCBI36
NG_054931.1:g.10052_10076delinsCTCCAGACCTTATCTGTGCAGCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.840+65_840+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3) MANE Select	ENSP00000373331.6:n.840+65_840+89delinsCTCCAGACCTTATCTGTGCAGC...
ENST00000433535.7:c.795+65_795+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	ENSP00000398921.3:n.795+65_795+89delinsCTCCAGACCTTATCTGTGCAGC...
ENST00000383820.9:c.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	ENSP00000373331.5:n.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGC...
ENST00000423108.5:c.397+18_397+42delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)
ENST00000424438.5:c.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	ENSP00000408693.1:n.629-760_629-736delinsCTCCAGACCTTATCTGTGCA...
ENST00000427174.5:c.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)
ENST00000433535.6:c.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	ENSP00000398921.2:n.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGC...
ENST00000455274.5:c.918+9548_918+9572delinsCAAGCTGCACAGATAAGGTCTGGAG (TTLL3)	ENSP00000409632.1:n.918+9548_918+9572delinsCAAGCTGCACAGATAAGG...
ENST00000464783.1:n.823+65_823+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)
ENST00000466141.1:n.682+65_682+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)
NM_001142547.1:c.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001136019.1:n.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGCTTG...
NM_173659.3:c.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_775930.2:n.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG
XM_011533627.1:c.725-760_725-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	XP_011531929.1:n.725-760_725-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001142547.2:c.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001136019.1:n.819+65_819+89delinsCTCCAGACCTTATCTGTGCAGCTTG...
NM_001351736.1:c.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338665.1:n.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001351737.1:c.725-760_725-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338666.1:n.725-760_725-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001351738.1:c.*22+65_*22+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338667.1:n.*22+65_*22+89delinsCTCCAGACCTTATCTGTGCAGCTTG...
NM_173659.4:c.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_775930.2:n.864+65_864+89delinsCTCCAGACCTTATCTGTGCAGCTTG
XM_024453471.1:c.911+18_911+42delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	XP_024309239.1:n.911+18_911+42delinsCTCCAGACCTTATCTGTGCAGCTTG...
XM_024453472.1:c.724+1217_724+1241delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	XP_024309240.1:n.724+1217_724+1241delinsCTCCAGACCTTATCTGTGCAG...
NM_001351736.2:c.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338665.1:n.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001351736.3:c.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338665.1:n.629-760_629-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001142547.3:c.795+65_795+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001136019.2:n.795+65_795+89delinsCTCCAGACCTTATCTGTGCAGCTTG...
NM_001351737.2:c.701-760_701-736delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338666.2:n.701-760_701-736delinsCTCCAGACCTTATCTGTGCAGCT...
NM_001351738.2:c.*22+65_*22+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3)	NP_001338667.2:n.*22+65_*22+89delinsCTCCAGACCTTATCTGTGCAGCTTG...
NM_173659.5:c.840+65_840+89delinsCTCCAGACCTTATCTGTGCAGCTTG (RPUSD3) MANE Select	NP_775930.3:n.840+65_840+89delinsCTCCAGACCTTATCTGTGCAGCTTG