Canonical Allele Identifier: CA2611365926

Gene: UROS

Linked Data

• gnomAD v4: 10-125812145-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125812148del , CM000672.2:g.125812148del	GRCh38
NC_000010.10:g.127500717del , CM000672.1:g.127500717del	GRCh37
NC_000010.9:g.127490707del	NCBI36
NG_011557.1:g.16123del
NG_011557.2:g.16123del

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.319+68del	ENSP00000518871.1:n.319+68del
ENST00000368797.10:c.319+68del MANE Select	ENSP00000357787.4:n.319+68del
ENST00000648119.1:c.319+68del	ENSP00000497494.1:n.319+68del
ENST00000648427.1:c.319+68del	ENSP00000497909.1:n.319+68del
ENST00000649275.1:c.248+68del
ENST00000649450.1:n.356+68del
ENST00000649536.1:c.319+68del	ENSP00000497817.1:n.319+68del
ENST00000650185.1:c.102+68del
ENST00000650524.1:c.124+68del	ENSP00000498108.1:n.124+68del
ENST00000650587.1:c.319+68del	ENSP00000497366.1:n.319+68del
ENST00000368774.1:c.319+68del	ENSP00000357763.1:n.319+68del
ENST00000368778.7:c.319+68del	ENSP00000357767.3:n.319+68del
ENST00000368786.5:c.319+68del	ENSP00000357775.1:n.319+68del
ENST00000368797.8:c.319+68del	ENSP00000357787.4:n.319+68del
ENST00000420761.5:c.235+68del	ENSP00000414833.1:n.235+68del
NM_000375.2:c.319+68del	NP_000366.1:n.319+68del
XM_005270137.2:c.319+68del	XP_005270194.1:n.319+68del
XM_005270138.2:c.319+68del	XP_005270195.1:n.319+68del
XM_005270139.2:c.319+68del	XP_005270196.1:n.319+68del
XM_005270140.3:c.319+68del	XP_005270197.1:n.319+68del
XM_005270141.1:c.319+68del	XP_005270198.1:n.319+68del
XM_006717960.2:c.319+68del	XP_006718023.1:n.319+68del
XM_011540126.1:c.319+68del	XP_011538428.1:n.319+68del
XM_011540127.1:c.319+68del	XP_011538429.1:n.319+68del
XR_246103.2:n.427+68del
XR_945809.1:n.427+68del
XR_945810.1:n.427+68del
NM_000375.3:c.319+68del MANE Select	NP_000366.1:n.319+68del
NM_001324036.1:c.319+68del	NP_001310965.1:n.319+68del
NM_001324037.1:c.319+68del	NP_001310966.1:n.319+68del
NM_001324038.1:c.319+68del	NP_001310967.1:n.319+68del
NM_001324039.1:c.319+68del	NP_001310968.1:n.319+68del
NR_136675.1:n.404+68del
NR_136676.1:n.585+68del
NR_136677.1:n.585+68del
NR_136678.1:n.315+68del
XM_005270140.5:c.319+68del	XP_005270197.1:n.319+68del
XM_011540127.2:c.319+68del	XP_011538429.1:n.319+68del
XM_017016611.2:c.319+68del	XP_016872100.2:n.319+68del
XM_017016612.2:c.319+68del	XP_016872101.1:n.319+68del
XM_024448154.1:c.319+68del	XP_024303922.1:n.319+68del
XM_024448155.1:c.319+68del	XP_024303923.1:n.319+68del
XR_001747196.2:n.442+68del
XR_001747197.2:n.442+68del
XR_002957009.1:n.442+68del
XR_002957010.1:n.383+68del
XR_246103.3:n.442+68del
XR_945810.2:n.442+68del
NM_001324036.2:c.319+68del	NP_001310965.1:n.319+68del
NM_001324037.2:c.319+68del	NP_001310966.1:n.319+68del
NM_001324038.2:c.319+68del	NP_001310967.1:n.319+68del
NR_136675.2:n.394+68del
NR_136676.2:n.575+68del
NR_136678.2:n.305+68del
NM_001324039.2:c.319+68del	NP_001310968.1:n.319+68del
NR_136677.2:n.575+68del