Canonical Allele Identifier: CA1344929440

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9838920A= , CM000665.2:g.9838920A=	GRCh38
NC_000003.11:g.9880604A= , CM000665.1:g.9880604A=	GRCh37
NC_000003.10:g.9855604A=	NCBI36
NG_054931.1:g.10099T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.840+112T= (RPUSD3) MANE Select	ENSP00000373331.6:n.840+112T=
ENST00000433535.7:c.795+112T= (RPUSD3)	ENSP00000398921.3:n.795+112T=
ENST00000383820.9:c.864+112T= (RPUSD3)	ENSP00000373331.5:n.864+112T=
ENST00000423108.5:c.397+65T= (RPUSD3)
ENST00000424438.5:c.629-713T= (RPUSD3)	ENSP00000408693.1:n.629-713T=
ENST00000427174.5:c.864+112T= (RPUSD3)
ENST00000433535.6:c.819+112T= (RPUSD3)	ENSP00000398921.2:n.819+112T=
ENST00000455274.5:c.918+9525A= (TTLL3)	ENSP00000409632.1:n.918+9525A=
ENST00000464783.1:n.823+112T= (RPUSD3)
ENST00000466141.1:n.682+112T= (RPUSD3)
NM_001142547.1:c.819+112T= (RPUSD3)	NP_001136019.1:n.819+112T=
NM_173659.3:c.864+112T= (RPUSD3)	NP_775930.2:n.864+112T=
XM_011533627.1:c.725-713T= (RPUSD3)	XP_011531929.1:n.725-713T=
NM_001142547.2:c.819+112T= (RPUSD3)	NP_001136019.1:n.819+112T=
NM_001351736.1:c.629-713T= (RPUSD3)	NP_001338665.1:n.629-713T=
NM_001351737.1:c.725-713T= (RPUSD3)	NP_001338666.1:n.725-713T=
NM_001351738.1:c.*22+112T= (RPUSD3)	NP_001338667.1:n.*22+112T=
NM_173659.4:c.864+112T= (RPUSD3)	NP_775930.2:n.864+112T=
XM_024453471.1:c.911+65T= (RPUSD3)	XP_024309239.1:n.911+65T=
XM_024453472.1:c.724+1264T= (RPUSD3)	XP_024309240.1:n.724+1264T=
NM_001351736.2:c.629-713T= (RPUSD3)	NP_001338665.1:n.629-713T=
NM_001351736.3:c.629-713T= (RPUSD3)	NP_001338665.1:n.629-713T=
NM_001142547.3:c.795+112T= (RPUSD3)	NP_001136019.2:n.795+112T=
NM_001351737.2:c.701-713T= (RPUSD3)	NP_001338666.2:n.701-713T=
NM_001351738.2:c.*22+112T= (RPUSD3)	NP_001338667.2:n.*22+112T=
NM_173659.5:c.840+112T= (RPUSD3) MANE Select	NP_775930.3:n.840+112T=