Canonical Allele Identifier: CA432388607

Gene: RPUSD3 TTLL3

Linked Data

• MyVariant Identifiers: chr3:g.9880845A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9839161A>G , CM000665.2:g.9839161A>G	GRCh38
NC_000003.11:g.9880845A>G , CM000665.1:g.9880845A>G	GRCh37
NC_000003.10:g.9855845A>G	NCBI36
NG_054931.1:g.9858T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000383820.10:c.711T>C (RPUSD3) MANE Select	ENSP00000373331.6:p.Ser237=
ENST00000433535.7:c.666T>C (RPUSD3)	ENSP00000398921.3:p.Ser222=
ENST00000383820.9:c.735T>C (RPUSD3)	ENSP00000373331.5:p.Ser245=
ENST00000423108.5:c.221T>C (RPUSD3)
ENST00000424438.5:c.629-954T>C (RPUSD3)	ENSP00000408693.1:n.629-954T>C
ENST00000427174.5:c.735T>C (RPUSD3)
ENST00000433535.6:c.690T>C (RPUSD3)	ENSP00000398921.2:p.Ser230=
ENST00000455274.5:c.918+9766A>G (TTLL3)	ENSP00000409632.1:n.918+9766A>G
ENST00000464783.1:n.694T>C (RPUSD3)
ENST00000466141.1:n.553T>C (RPUSD3)
NM_001142547.1:c.690T>C (RPUSD3)	NP_001136019.1:p.Ser230=
NM_173659.3:c.735T>C (RPUSD3)	NP_775930.2:p.Ser245=
XM_011533627.1:c.725-954T>C (RPUSD3)	XP_011531929.1:n.725-954T>C
NM_001142547.2:c.690T>C (RPUSD3)	NP_001136019.1:p.Ser230=
NM_001351736.1:c.629-954T>C (RPUSD3)	NP_001338665.1:n.629-954T>C
NM_001351737.1:c.725-954T>C (RPUSD3)	NP_001338666.1:n.725-954T>C
NM_001351738.1:c.763T>C (RPUSD3)	NP_001338667.1:p.Ser255Pro
NM_173659.4:c.735T>C (RPUSD3)	NP_775930.2:p.Ser245=
XM_024453471.1:c.735T>C (RPUSD3)	XP_024309239.1:p.Ser245=
XM_024453472.1:c.724+1023T>C (RPUSD3)	XP_024309240.1:n.724+1023T>C
NM_001351736.2:c.629-954T>C (RPUSD3)	NP_001338665.1:n.629-954T>C
NM_001351736.3:c.629-954T>C (RPUSD3)	NP_001338665.1:n.629-954T>C
NM_001142547.3:c.666T>C (RPUSD3)	NP_001136019.2:p.Ser222=
NM_001351737.2:c.701-954T>C (RPUSD3)	NP_001338666.2:n.701-954T>C
NM_001351738.2:c.739T>C (RPUSD3)	NP_001338667.2:p.Ser247Pro
NM_173659.5:c.711T>C (RPUSD3) MANE Select	NP_775930.3:p.Ser237=