Canonical Allele Identifier: CA1344929676

Gene: RPUSD3 TTLL3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839126G= , CM000665.2:g.9839126G=	GRCh38
NC_000003.11:g.9880810G= , CM000665.1:g.9880810G=	GRCh37
NC_000003.10:g.9855810G=	NCBI36
NG_054931.1:g.9893C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.746C= (RPUSD3) MANE Select	ENSP00000373331.6:p.Pro249=
ENST00000433535.7:c.701C= (RPUSD3)	ENSP00000398921.3:p.Pro234=
ENST00000383820.9:c.770C= (RPUSD3)	ENSP00000373331.5:p.Pro257=
ENST00000423108.5:c.256C= (RPUSD3)
ENST00000424438.5:c.629-919C= (RPUSD3)	ENSP00000408693.1:n.629-919C=
ENST00000427174.5:c.770C= (RPUSD3)
ENST00000433535.6:c.725C= (RPUSD3)	ENSP00000398921.2:p.Pro242=
ENST00000455274.5:c.918+9731G= (TTLL3)	ENSP00000409632.1:n.918+9731G=
ENST00000464783.1:n.729C= (RPUSD3)
ENST00000466141.1:n.588C= (RPUSD3)
NM_001142547.1:c.725C= (RPUSD3)	NP_001136019.1:p.Pro242=
NM_173659.3:c.770C= (RPUSD3)	NP_775930.2:p.Pro257=
XM_011533627.1:c.725-919C= (RPUSD3)	XP_011531929.1:n.725-919C=
NM_001142547.2:c.725C= (RPUSD3)	NP_001136019.1:p.Pro242=
NM_001351736.1:c.629-919C= (RPUSD3)	NP_001338665.1:n.629-919C=
NM_001351737.1:c.725-919C= (RPUSD3)	NP_001338666.1:n.725-919C=
NM_001351738.1:c.798C= (RPUSD3)	NP_001338667.1:p.Pro266=
NM_173659.4:c.770C= (RPUSD3)	NP_775930.2:p.Pro257=
XM_024453471.1:c.770C= (RPUSD3)	XP_024309239.1:p.Pro257=
XM_024453472.1:c.724+1058C= (RPUSD3)	XP_024309240.1:n.724+1058C=
NM_001351736.2:c.629-919C= (RPUSD3)	NP_001338665.1:n.629-919C=
NM_001351736.3:c.629-919C= (RPUSD3)	NP_001338665.1:n.629-919C=
NM_001142547.3:c.701C= (RPUSD3)	NP_001136019.2:p.Pro234=
NM_001351737.2:c.701-919C= (RPUSD3)	NP_001338666.2:n.701-919C=
NM_001351738.2:c.774C= (RPUSD3)	NP_001338667.2:p.Pro258=
NM_173659.5:c.746C= (RPUSD3) MANE Select	NP_775930.3:p.Pro249=