Canonical Allele Identifier: CA1344929727

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839148G= , CM000665.2:g.9839148G=	GRCh38
NC_000003.11:g.9880832G= , CM000665.1:g.9880832G=	GRCh37
NC_000003.10:g.9855832G=	NCBI36
NG_054931.1:g.9871C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000383820.10:c.724C= (RPUSD3) MANE Select	ENSP00000373331.6:p.His242=
ENST00000433535.7:c.679C= (RPUSD3)	ENSP00000398921.3:p.His227=
ENST00000383820.9:c.748C= (RPUSD3)	ENSP00000373331.5:p.His250=
ENST00000423108.5:c.234C= (RPUSD3)
ENST00000424438.5:c.629-941C= (RPUSD3)	ENSP00000408693.1:n.629-941C=
ENST00000427174.5:c.748C= (RPUSD3)
ENST00000433535.6:c.703C= (RPUSD3)	ENSP00000398921.2:p.His235=
ENST00000455274.5:c.918+9753G= (TTLL3)	ENSP00000409632.1:n.918+9753G=
ENST00000464783.1:n.707C= (RPUSD3)
ENST00000466141.1:n.566C= (RPUSD3)
NM_001142547.1:c.703C= (RPUSD3)	NP_001136019.1:p.His235=
NM_173659.3:c.748C= (RPUSD3)	NP_775930.2:p.His250=
XM_011533627.1:c.725-941C= (RPUSD3)	XP_011531929.1:n.725-941C=
NM_001142547.2:c.703C= (RPUSD3)	NP_001136019.1:p.His235=
NM_001351736.1:c.629-941C= (RPUSD3)	NP_001338665.1:n.629-941C=
NM_001351737.1:c.725-941C= (RPUSD3)	NP_001338666.1:n.725-941C=
NM_001351738.1:c.776C= (RPUSD3)	NP_001338667.1:p.Ala259=
NM_173659.4:c.748C= (RPUSD3)	NP_775930.2:p.His250=
XM_024453471.1:c.748C= (RPUSD3)	XP_024309239.1:p.His250=
XM_024453472.1:c.724+1036C= (RPUSD3)	XP_024309240.1:n.724+1036C=
NM_001351736.2:c.629-941C= (RPUSD3)	NP_001338665.1:n.629-941C=
NM_001351736.3:c.629-941C= (RPUSD3)	NP_001338665.1:n.629-941C=
NM_001142547.3:c.679C= (RPUSD3)	NP_001136019.2:p.His227=
NM_001351737.2:c.701-941C= (RPUSD3)	NP_001338666.2:n.701-941C=
NM_001351738.2:c.752C= (RPUSD3)	NP_001338667.2:p.Ala251=
NM_173659.5:c.724C= (RPUSD3) MANE Select	NP_775930.3:p.His242=