Canonical Allele Identifier: CA1943004031

Gene: UROS

Linked Data

• dbSNP Id: rs1851237160

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125794979_125794980del , CM000672.2:g.125794979_125794980del	GRCh38
NC_000010.10:g.127483548_127483549del , CM000672.1:g.127483548_127483549del	GRCh37
NC_000010.9:g.127473538_127473539del	NCBI36
NG_011557.1:g.33289_33290del
NG_011557.2:g.33289_33290del

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.562-2_562-1del	ENSP00000518871.1:n.562-2_562-1del
ENST00000368797.10:c.562-2_562-1del MANE Select	ENSP00000357787.4:n.562-2_562-1del
ENST00000465577.6:c.336-2_336-1del
ENST00000648119.1:c.*151-2_*151-1del	ENSP00000497494.1:n.*151-2_*151-1del
ENST00000648427.1:c.*314-2_*314-1del	ENSP00000497909.1:n.*314-2_*314-1del
ENST00000649275.1:c.577-2_577-1del
ENST00000649536.1:c.481-2_481-1del	ENSP00000497817.1:n.481-2_481-1del
ENST00000650185.1:c.345-2_345-1del
ENST00000650472.1:n.2948-2_2948-1del
ENST00000650524.1:c.475-2_475-1del	ENSP00000498108.1:n.475-2_475-1del
ENST00000650587.1:c.562-2_562-1del	ENSP00000497366.1:n.562-2_562-1del
ENST00000368786.5:c.562-2_562-1del	ENSP00000357775.1:n.562-2_562-1del
ENST00000368797.8:c.562-2_562-1del	ENSP00000357787.4:n.562-2_562-1del
ENST00000420761.5:c.478-2_478-1del	ENSP00000414833.1:n.478-2_478-1del
ENST00000462490.5:c.221-2_221-1del
ENST00000464267.1:n.126-2_126-1del
ENST00000465577.5:n.123-2_123-1del
ENST00000470483.1:n.248_249del
ENST00000484541.5:n.89-2_89-1del
ENST00000616800.4:c.62-2_62-1del
ENST00000622016.4:c.142-2_142-1del	ENSP00000483041.1:n.142-2_142-1del
NM_000375.2:c.562-2_562-1del	NP_000366.1:n.562-2_562-1del
XM_005270137.2:c.562-2_562-1del	XP_005270194.1:n.562-2_562-1del
XM_005270138.2:c.481-2_481-1del	XP_005270195.1:n.481-2_481-1del
XM_005270139.2:c.562-2_562-1del	XP_005270196.1:n.562-2_562-1del
XM_005270140.3:c.562-2_562-1del	XP_005270197.1:n.562-2_562-1del
XM_006717960.2:c.562-2_562-1del	XP_006718023.1:n.562-2_562-1del
XM_011540126.1:c.562-2_562-1del	XP_011538428.1:n.562-2_562-1del
XM_011540127.1:c.562-2_562-1del	XP_011538429.1:n.562-2_562-1del
XR_246103.2:n.742-2_742-1del
XR_945809.1:n.670-2_670-1del
XR_945810.1:n.972-2_972-1del
NM_000375.3:c.562-2_562-1del MANE Select	NP_000366.1:n.562-2_562-1del
NM_001324036.1:c.562-2_562-1del	NP_001310965.1:n.562-2_562-1del
NM_001324037.1:c.481-2_481-1del	NP_001310966.1:n.481-2_481-1del
NM_001324038.1:c.481-2_481-1del	NP_001310967.1:n.481-2_481-1del
NR_136675.1:n.647-2_647-1del
NR_136676.1:n.828-2_828-1del
NR_136677.1:n.828-2_828-1del
NR_136678.1:n.558-2_558-1del
XM_005270140.5:c.562-2_562-1del	XP_005270197.1:n.562-2_562-1del
XM_011540127.2:c.562-2_562-1del	XP_011538429.1:n.562-2_562-1del
XM_017016611.2:c.562-2_562-1del	XP_016872100.2:n.562-2_562-1del
XM_017016612.2:c.562-2_562-1del	XP_016872101.1:n.562-2_562-1del
XM_024448154.1:c.562-2_562-1del	XP_024303922.1:n.562-2_562-1del
XM_024448155.1:c.481-2_481-1del	XP_024303923.1:n.481-2_481-1del
XR_001747196.2:n.685-2_685-1del
XR_001747197.2:n.757-2_757-1del
XR_002957009.1:n.685-2_685-1del
XR_002957010.1:n.1901-2_1901-1del
XR_246103.3:n.757-2_757-1del
XR_945810.2:n.987-2_987-1del
NM_001324036.2:c.562-2_562-1del	NP_001310965.1:n.562-2_562-1del
NM_001324037.2:c.481-2_481-1del	NP_001310966.1:n.481-2_481-1del
NM_001324038.2:c.481-2_481-1del	NP_001310967.1:n.481-2_481-1del
NR_136675.2:n.637-2_637-1del
NR_136676.2:n.818-2_818-1del
NR_136678.2:n.548-2_548-1del
NR_136677.2:n.818-2_818-1del