Canonical Allele Identifier: CA351734257

Gene: RPUSD3 TTLL3

Linked Data

• MyVariant Identifiers: chr3:g.9880832G>C (hg19) ; chr3:g.9839148G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000383820.10:c.724C>G (RPUSD3) MANE Select	ENSP00000373331.6:p.His242Asp
ENST00000433535.7:c.679C>G (RPUSD3)	ENSP00000398921.3:p.His227Asp
ENST00000383820.9:c.748C>G (RPUSD3)	ENSP00000373331.5:p.His250Asp
ENST00000423108.5:c.234C>G (RPUSD3)
ENST00000424438.5:c.629-941C>G (RPUSD3)	ENSP00000408693.1:n.629-941C>G
ENST00000427174.5:c.748C>G (RPUSD3)
ENST00000433535.6:c.703C>G (RPUSD3)	ENSP00000398921.2:p.His235Asp
ENST00000455274.5:c.918+9753G>C (TTLL3)	ENSP00000409632.1:n.918+9753G>C
ENST00000464783.1:n.707C>G (RPUSD3)
ENST00000466141.1:n.566C>G (RPUSD3)
NM_001142547.1:c.703C>G (RPUSD3)	NP_001136019.1:p.His235Asp
NM_173659.3:c.748C>G (RPUSD3)	NP_775930.2:p.His250Asp
XM_011533627.1:c.725-941C>G (RPUSD3)	XP_011531929.1:n.725-941C>G
NM_001142547.2:c.703C>G (RPUSD3)	NP_001136019.1:p.His235Asp
NM_001351736.1:c.629-941C>G (RPUSD3)	NP_001338665.1:n.629-941C>G
NM_001351737.1:c.725-941C>G (RPUSD3)	NP_001338666.1:n.725-941C>G
NM_001351738.1:c.776C>G (RPUSD3)	NP_001338667.1:p.Ala259Gly
NM_173659.4:c.748C>G (RPUSD3)	NP_775930.2:p.His250Asp
XM_024453471.1:c.748C>G (RPUSD3)	XP_024309239.1:p.His250Asp
XM_024453472.1:c.724+1036C>G (RPUSD3)	XP_024309240.1:n.724+1036C>G
NM_001351736.2:c.629-941C>G (RPUSD3)	NP_001338665.1:n.629-941C>G
NM_001351736.3:c.629-941C>G (RPUSD3)	NP_001338665.1:n.629-941C>G
NM_001142547.3:c.679C>G (RPUSD3)	NP_001136019.2:p.His227Asp
NM_001351737.2:c.701-941C>G (RPUSD3)	NP_001338666.2:n.701-941C>G
NM_001351738.2:c.752C>G (RPUSD3)	NP_001338667.2:p.Ala251Gly
NM_173659.5:c.724C>G (RPUSD3) MANE Select	NP_775930.3:p.His242Asp