Canonical Allele Identifier: CA661180938

Gene: UROS

Linked Data

• dbSNP Id: rs1230600743
• gnomAD v3: 10-125816348-GA-G
• gnomAD v4: 10-125816348-GA-G
• MyVariant Identifiers: chr10:g.127504918del (hg19) ; chr10:g.125816349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125816349del , CM000672.2:g.125816349del	GRCh38
NC_000010.10:g.127504918del , CM000672.1:g.127504918del	GRCh37
NC_000010.9:g.127494908del	NCBI36
NG_011557.1:g.11920del
NG_011557.2:g.11920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.64-89del	ENSP00000518871.1:n.64-89del
ENST00000368797.10:c.64-89del MANE Select	ENSP00000357787.4:n.64-89del
ENST00000648119.1:c.64-89del	ENSP00000497494.1:n.64-89del
ENST00000648427.1:c.64-89del	ENSP00000497909.1:n.64-89del
ENST00000649450.1:n.101-89del
ENST00000649536.1:c.64-89del	ENSP00000497817.1:n.64-89del
ENST00000650587.1:c.64-89del	ENSP00000497366.1:n.64-89del
ENST00000368774.1:c.64-89del	ENSP00000357763.1:n.64-89del
ENST00000368778.7:c.64-89del	ENSP00000357767.3:n.64-89del
ENST00000368786.5:c.64-89del	ENSP00000357775.1:n.64-89del
ENST00000368797.8:c.64-89del	ENSP00000357787.4:n.64-89del
ENST00000420761.5:c.63+88del	ENSP00000414833.1:n.63+88del
NM_000375.2:c.64-89del	NP_000366.1:n.64-89del
XM_005270137.2:c.64-89del	XP_005270194.1:n.64-89del
XM_005270138.2:c.64-89del	XP_005270195.1:n.64-89del
XM_005270139.2:c.64-89del	XP_005270196.1:n.64-89del
XM_005270140.3:c.64-89del	XP_005270197.1:n.64-89del
XM_005270141.1:c.64-89del	XP_005270198.1:n.64-89del
XM_006717960.2:c.64-89del	XP_006718023.1:n.64-89del
XM_011540126.1:c.64-89del	XP_011538428.1:n.64-89del
XM_011540127.1:c.64-89del	XP_011538429.1:n.64-89del
XR_246103.2:n.172-89del
XR_945809.1:n.172-89del
XR_945810.1:n.172-89del
NM_000375.3:c.64-89del MANE Select	NP_000366.1:n.64-89del
NM_001324036.1:c.64-89del	NP_001310965.1:n.64-89del
NM_001324037.1:c.64-89del	NP_001310966.1:n.64-89del
NM_001324038.1:c.64-89del	NP_001310967.1:n.64-89del
NM_001324039.1:c.64-89del	NP_001310968.1:n.64-89del
NR_136675.1:n.329+88del
NR_136676.1:n.330-89del
NR_136677.1:n.330-89del
NR_136678.1:n.241-4061del
XM_005270140.5:c.64-89del	XP_005270197.1:n.64-89del
XM_011540127.2:c.64-89del	XP_011538429.1:n.64-89del
XM_017016611.2:c.64-89del	XP_016872100.2:n.64-89del
XM_017016612.2:c.64-89del	XP_016872101.1:n.64-89del
XM_024448154.1:c.64-89del	XP_024303922.1:n.64-89del
XM_024448155.1:c.64-89del	XP_024303923.1:n.64-89del
XR_001747196.2:n.187-89del
XR_001747197.2:n.187-89del
XR_002957009.1:n.187-89del
XR_002957010.1:n.128-89del
XR_246103.3:n.187-89del
XR_945810.2:n.187-89del
NM_001324036.2:c.64-89del	NP_001310965.1:n.64-89del
NM_001324037.2:c.64-89del	NP_001310966.1:n.64-89del
NM_001324038.2:c.64-89del	NP_001310967.1:n.64-89del
NR_136675.2:n.319+88del
NR_136676.2:n.320-89del
NR_136678.2:n.231-4061del
NM_001324039.2:c.64-89del	NP_001310968.1:n.64-89del
NR_136677.2:n.320-89del