Canonical Allele Identifier: CA1344929584

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839044_9839047delinsCTTG , CM000665.2:g.9839044_9839047delinsCTTG	GRCh38
NC_000003.11:g.9880728_9880731delinsCTTG , CM000665.1:g.9880728_9880731delinsCTTG	GRCh37
NC_000003.10:g.9855728_9855731delinsCTTG	NCBI36
NG_054931.1:g.9972_9975delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.825_828delinsCAAG (RPUSD3) MANE Select	ENSP00000373331.6:p.Asn275=
ENST00000433535.7:c.780_783delinsCAAG (RPUSD3)	ENSP00000398921.3:p.Asn260=
ENST00000383820.9:c.849_852delinsCAAG (RPUSD3)	ENSP00000373331.5:p.Asn283=
ENST00000423108.5:c.335_338delinsCAAG (RPUSD3)
ENST00000424438.5:c.629-840_629-837delinsCAAG (RPUSD3)	ENSP00000408693.1:n.629-840_629-837delinsCAAG
ENST00000427174.5:c.849_852delinsCAAG (RPUSD3)
ENST00000433535.6:c.804_807delinsCAAG (RPUSD3)	ENSP00000398921.2:p.Asn268=
ENST00000455274.5:c.918+9649_918+9652delinsCTTG (TTLL3)	ENSP00000409632.1:n.918+9649_918+9652delinsCTTG
ENST00000464783.1:n.808_811delinsCAAG (RPUSD3)
ENST00000466141.1:n.667_670delinsCAAG (RPUSD3)
NM_001142547.1:c.804_807delinsCAAG (RPUSD3)	NP_001136019.1:p.Asn268=
NM_173659.3:c.849_852delinsCAAG (RPUSD3)	NP_775930.2:p.Asn283=
XM_011533627.1:c.725-840_725-837delinsCAAG (RPUSD3)	XP_011531929.1:n.725-840_725-837delinsCAAG
NM_001142547.2:c.804_807delinsCAAG (RPUSD3)	NP_001136019.1:p.Asn268=
NM_001351736.1:c.629-840_629-837delinsCAAG (RPUSD3)	NP_001338665.1:n.629-840_629-837delinsCAAG
NM_001351737.1:c.725-840_725-837delinsCAAG (RPUSD3)	NP_001338666.1:n.725-840_725-837delinsCAAG
NM_001351738.1:c.*7_*10delinsCAAG (RPUSD3)	NP_001338667.1:n.*7_*10delinsCAAG
NM_173659.4:c.849_852delinsCAAG (RPUSD3)	NP_775930.2:p.Asn283=
XM_024453471.1:c.849_852delinsCAAG (RPUSD3)	XP_024309239.1:p.Asn283=
XM_024453472.1:c.724+1137_724+1140delinsCAAG (RPUSD3)	XP_024309240.1:n.724+1137_724+1140delinsCAAG
NM_001351736.2:c.629-840_629-837delinsCAAG (RPUSD3)	NP_001338665.1:n.629-840_629-837delinsCAAG
NM_001351736.3:c.629-840_629-837delinsCAAG (RPUSD3)	NP_001338665.1:n.629-840_629-837delinsCAAG
NM_001142547.3:c.780_783delinsCAAG (RPUSD3)	NP_001136019.2:p.Asn260=
NM_001351737.2:c.701-840_701-837delinsCAAG (RPUSD3)	NP_001338666.2:n.701-840_701-837delinsCAAG
NM_001351738.2:c.*7_*10delinsCAAG (RPUSD3)	NP_001338667.2:n.*7_*10delinsCAAG
NM_173659.5:c.825_828delinsCAAG (RPUSD3) MANE Select	NP_775930.3:p.Asn275=