Canonical Allele Identifier: CA432388488

Gene: RPUSD3 TTLL3

Linked Data

• MyVariant Identifiers: chr3:g.9880725G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839041G>C , CM000665.2:g.9839041G>C	GRCh38
NC_000003.11:g.9880725G>C , CM000665.1:g.9880725G>C	GRCh37
NC_000003.10:g.9855725G>C	NCBI36
NG_054931.1:g.9978C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.831C>G (RPUSD3) MANE Select	ENSP00000373331.6:p.Pro277=
ENST00000433535.7:c.786C>G (RPUSD3)	ENSP00000398921.3:p.Pro262=
ENST00000383820.9:c.855C>G (RPUSD3)	ENSP00000373331.5:p.Pro285=
ENST00000423108.5:c.341C>G (RPUSD3)
ENST00000424438.5:c.629-834C>G (RPUSD3)	ENSP00000408693.1:n.629-834C>G
ENST00000427174.5:c.855C>G (RPUSD3)
ENST00000433535.6:c.810C>G (RPUSD3)	ENSP00000398921.2:p.Pro270=
ENST00000455274.5:c.918+9646G>C (TTLL3)	ENSP00000409632.1:n.918+9646G>C
ENST00000464783.1:n.814C>G (RPUSD3)
ENST00000466141.1:n.673C>G (RPUSD3)
NM_001142547.1:c.810C>G (RPUSD3)	NP_001136019.1:p.Pro270=
NM_173659.3:c.855C>G (RPUSD3)	NP_775930.2:p.Pro285=
XM_011533627.1:c.725-834C>G (RPUSD3)	XP_011531929.1:n.725-834C>G
NM_001142547.2:c.810C>G (RPUSD3)	NP_001136019.1:p.Pro270=
NM_001351736.1:c.629-834C>G (RPUSD3)	NP_001338665.1:n.629-834C>G
NM_001351737.1:c.725-834C>G (RPUSD3)	NP_001338666.1:n.725-834C>G
NM_001351738.1:c.*13C>G (RPUSD3)	NP_001338667.1:n.*13C>G
NM_173659.4:c.855C>G (RPUSD3)	NP_775930.2:p.Pro285=
XM_024453471.1:c.855C>G (RPUSD3)	XP_024309239.1:p.Pro285=
XM_024453472.1:c.724+1143C>G (RPUSD3)	XP_024309240.1:n.724+1143C>G
NM_001351736.2:c.629-834C>G (RPUSD3)	NP_001338665.1:n.629-834C>G
NM_001351736.3:c.629-834C>G (RPUSD3)	NP_001338665.1:n.629-834C>G
NM_001142547.3:c.786C>G (RPUSD3)	NP_001136019.2:p.Pro262=
NM_001351737.2:c.701-834C>G (RPUSD3)	NP_001338666.2:n.701-834C>G
NM_001351738.2:c.*13C>G (RPUSD3)	NP_001338667.2:n.*13C>G
NM_173659.5:c.831C>G (RPUSD3) MANE Select	NP_775930.3:p.Pro277=