Canonical Allele Identifier: CA351734008

Gene: RPUSD3 TTLL3

Linked Data

• MyVariant Identifiers: chr3:g.9880796G>T (hg19) ; chr3:g.9839112G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839112G>T , CM000665.2:g.9839112G>T	GRCh38
NC_000003.11:g.9880796G>T , CM000665.1:g.9880796G>T	GRCh37
NC_000003.10:g.9855796G>T	NCBI36
NG_054931.1:g.9907C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383820.10:c.760C>A (RPUSD3) MANE Select	ENSP00000373331.6:p.His254Asn
ENST00000433535.7:c.715C>A (RPUSD3)	ENSP00000398921.3:p.His239Asn
ENST00000383820.9:c.784C>A (RPUSD3)	ENSP00000373331.5:p.His262Asn
ENST00000423108.5:c.270C>A (RPUSD3)
ENST00000424438.5:c.629-905C>A (RPUSD3)	ENSP00000408693.1:n.629-905C>A
ENST00000427174.5:c.784C>A (RPUSD3)
ENST00000433535.6:c.739C>A (RPUSD3)	ENSP00000398921.2:p.His247Asn
ENST00000455274.5:c.918+9717G>T (TTLL3)	ENSP00000409632.1:n.918+9717G>T
ENST00000464783.1:n.743C>A (RPUSD3)
ENST00000466141.1:n.602C>A (RPUSD3)
NM_001142547.1:c.739C>A (RPUSD3)	NP_001136019.1:p.His247Asn
NM_173659.3:c.784C>A (RPUSD3)	NP_775930.2:p.His262Asn
XM_011533627.1:c.725-905C>A (RPUSD3)	XP_011531929.1:n.725-905C>A
NM_001142547.2:c.739C>A (RPUSD3)	NP_001136019.1:p.His247Asn
NM_001351736.1:c.629-905C>A (RPUSD3)	NP_001338665.1:n.629-905C>A
NM_001351737.1:c.725-905C>A (RPUSD3)	NP_001338666.1:n.725-905C>A
NM_001351738.1:c.812C>A (RPUSD3)	NP_001338667.1:p.Pro271Gln
NM_173659.4:c.784C>A (RPUSD3)	NP_775930.2:p.His262Asn
XM_024453471.1:c.784C>A (RPUSD3)	XP_024309239.1:p.His262Asn
XM_024453472.1:c.724+1072C>A (RPUSD3)	XP_024309240.1:n.724+1072C>A
NM_001351736.2:c.629-905C>A (RPUSD3)	NP_001338665.1:n.629-905C>A
NM_001351736.3:c.629-905C>A (RPUSD3)	NP_001338665.1:n.629-905C>A
NM_001142547.3:c.715C>A (RPUSD3)	NP_001136019.2:p.His239Asn
NM_001351737.2:c.701-905C>A (RPUSD3)	NP_001338666.2:n.701-905C>A
NM_001351738.2:c.788C>A (RPUSD3)	NP_001338667.2:p.Pro263Gln
NM_173659.5:c.760C>A (RPUSD3) MANE Select	NP_775930.3:p.His254Asn