Canonical Allele Identifier: CA1943010556

Gene: UROS

Linked Data

• dbSNP Id: rs1853322654

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125816396_125816399del , CM000672.2:g.125816396_125816399del	GRCh38
NC_000010.10:g.127504965_127504968del , CM000672.1:g.127504965_127504968del	GRCh37
NC_000010.9:g.127494955_127494958del	NCBI36
NG_011557.1:g.11870_11873del
NG_011557.2:g.11870_11873del

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.63+38_63+41del	ENSP00000518871.1:n.63+38_63+41del
ENST00000368797.10:c.63+38_63+41del MANE Select	ENSP00000357787.4:n.63+38_63+41del
ENST00000648119.1:c.63+38_63+41del	ENSP00000497494.1:n.63+38_63+41del
ENST00000648427.1:c.63+38_63+41del	ENSP00000497909.1:n.63+38_63+41del
ENST00000649450.1:n.100+38_100+41del
ENST00000649536.1:c.63+38_63+41del	ENSP00000497817.1:n.63+38_63+41del
ENST00000650587.1:c.63+38_63+41del	ENSP00000497366.1:n.63+38_63+41del
ENST00000368774.1:c.63+38_63+41del	ENSP00000357763.1:n.63+38_63+41del
ENST00000368778.7:c.63+38_63+41del	ENSP00000357767.3:n.63+38_63+41del
ENST00000368786.5:c.63+38_63+41del	ENSP00000357775.1:n.63+38_63+41del
ENST00000368797.8:c.63+38_63+41del	ENSP00000357787.4:n.63+38_63+41del
ENST00000420761.5:c.63+38_63+41del	ENSP00000414833.1:n.63+38_63+41del
NM_000375.2:c.63+38_63+41del	NP_000366.1:n.63+38_63+41del
XM_005270137.2:c.63+38_63+41del	XP_005270194.1:n.63+38_63+41del
XM_005270138.2:c.63+38_63+41del	XP_005270195.1:n.63+38_63+41del
XM_005270139.2:c.63+38_63+41del	XP_005270196.1:n.63+38_63+41del
XM_005270140.3:c.63+38_63+41del	XP_005270197.1:n.63+38_63+41del
XM_005270141.1:c.63+38_63+41del	XP_005270198.1:n.63+38_63+41del
XM_006717960.2:c.63+38_63+41del	XP_006718023.1:n.63+38_63+41del
XM_011540126.1:c.63+38_63+41del	XP_011538428.1:n.63+38_63+41del
XM_011540127.1:c.63+38_63+41del	XP_011538429.1:n.63+38_63+41del
XR_246103.2:n.171+38_171+41del
XR_945809.1:n.171+38_171+41del
XR_945810.1:n.171+38_171+41del
NM_000375.3:c.63+38_63+41del MANE Select	NP_000366.1:n.63+38_63+41del
NM_001324036.1:c.63+38_63+41del	NP_001310965.1:n.63+38_63+41del
NM_001324037.1:c.63+38_63+41del	NP_001310966.1:n.63+38_63+41del
NM_001324038.1:c.63+38_63+41del	NP_001310967.1:n.63+38_63+41del
NM_001324039.1:c.63+38_63+41del	NP_001310968.1:n.63+38_63+41del
NR_136675.1:n.329+38_329+41del
NR_136676.1:n.329+38_329+41del
NR_136677.1:n.329+38_329+41del
NR_136678.1:n.241-4111_241-4108del
XM_005270140.5:c.63+38_63+41del	XP_005270197.1:n.63+38_63+41del
XM_011540127.2:c.63+38_63+41del	XP_011538429.1:n.63+38_63+41del
XM_017016611.2:c.63+38_63+41del	XP_016872100.2:n.63+38_63+41del
XM_017016612.2:c.63+38_63+41del	XP_016872101.1:n.63+38_63+41del
XM_024448154.1:c.63+38_63+41del	XP_024303922.1:n.63+38_63+41del
XM_024448155.1:c.63+38_63+41del	XP_024303923.1:n.63+38_63+41del
XR_001747196.2:n.186+38_186+41del
XR_001747197.2:n.186+38_186+41del
XR_002957009.1:n.186+38_186+41del
XR_002957010.1:n.127+38_127+41del
XR_246103.3:n.186+38_186+41del
XR_945810.2:n.186+38_186+41del
NM_001324036.2:c.63+38_63+41del	NP_001310965.1:n.63+38_63+41del
NM_001324037.2:c.63+38_63+41del	NP_001310966.1:n.63+38_63+41del
NM_001324038.2:c.63+38_63+41del	NP_001310967.1:n.63+38_63+41del
NR_136675.2:n.319+38_319+41del
NR_136676.2:n.319+38_319+41del
NR_136678.2:n.231-4111_231-4108del
NM_001324039.2:c.63+38_63+41del	NP_001310968.1:n.63+38_63+41del
NR_136677.2:n.319+38_319+41del