Canonical Allele Identifier: CA1344929630

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839093A= , CM000665.2:g.9839093A=	GRCh38
NC_000003.11:g.9880777A= , CM000665.1:g.9880777A=	GRCh37
NC_000003.10:g.9855777A=	NCBI36
NG_054931.1:g.9926T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.779T= (RPUSD3) MANE Select	ENSP00000373331.6:p.Val260=
ENST00000433535.7:c.734T= (RPUSD3)	ENSP00000398921.3:p.Val245=
ENST00000383820.9:c.803T= (RPUSD3)	ENSP00000373331.5:p.Val268=
ENST00000423108.5:c.289T= (RPUSD3)
ENST00000424438.5:c.629-886T= (RPUSD3)	ENSP00000408693.1:n.629-886T=
ENST00000427174.5:c.803T= (RPUSD3)
ENST00000433535.6:c.758T= (RPUSD3)	ENSP00000398921.2:p.Val253=
ENST00000455274.5:c.918+9698A= (TTLL3)	ENSP00000409632.1:n.918+9698A=
ENST00000464783.1:n.762T= (RPUSD3)
ENST00000466141.1:n.621T= (RPUSD3)
NM_001142547.1:c.758T= (RPUSD3)	NP_001136019.1:p.Val253=
NM_173659.3:c.803T= (RPUSD3)	NP_775930.2:p.Val268=
XM_011533627.1:c.725-886T= (RPUSD3)	XP_011531929.1:n.725-886T=
NM_001142547.2:c.758T= (RPUSD3)	NP_001136019.1:p.Val253=
NM_001351736.1:c.629-886T= (RPUSD3)	NP_001338665.1:n.629-886T=
NM_001351737.1:c.725-886T= (RPUSD3)	NP_001338666.1:n.725-886T=
NM_001351738.1:c.831T= (RPUSD3)	NP_001338667.1:p.Cys277=
NM_173659.4:c.803T= (RPUSD3)	NP_775930.2:p.Val268=
XM_024453471.1:c.803T= (RPUSD3)	XP_024309239.1:p.Val268=
XM_024453472.1:c.724+1091T= (RPUSD3)	XP_024309240.1:n.724+1091T=
NM_001351736.2:c.629-886T= (RPUSD3)	NP_001338665.1:n.629-886T=
NM_001351736.3:c.629-886T= (RPUSD3)	NP_001338665.1:n.629-886T=
NM_001142547.3:c.734T= (RPUSD3)	NP_001136019.2:p.Val245=
NM_001351737.2:c.701-886T= (RPUSD3)	NP_001338666.2:n.701-886T=
NM_001351738.2:c.807T= (RPUSD3)	NP_001338667.2:p.Cys269=
NM_173659.5:c.779T= (RPUSD3) MANE Select	NP_775930.3:p.Val260=