Canonical Allele Identifier: CA1943001140

Gene: UROS

Linked Data

• dbSNP Id: rs1850711679
• gnomAD v4: 10-125788764-GAGTCTGACGGCAGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125788767_125788780del , CM000672.2:g.125788767_125788780del	GRCh38
NC_000010.10:g.127477336_127477349del , CM000672.1:g.127477336_127477349del	GRCh37
NC_000010.9:g.127467326_127467339del	NCBI36
NG_011557.1:g.39491_39504del
NG_011557.2:g.39491_39504del

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.*90_*103del	ENSP00000518871.1:n.*90_*103del
ENST00000368797.10:c.*90_*103del MANE Select	ENSP00000357787.4:n.*90_*103del
ENST00000465577.6:c.908_921del
ENST00000648427.1:c.*886_*899del	ENSP00000497909.1:n.*886_*899del
ENST00000649536.1:c.*90_*103del	ENSP00000497817.1:n.*90_*103del
ENST00000650472.1:n.3274_3287del
ENST00000650524.1:c.801_814del	ENSP00000498108.1:n.801_814del
ENST00000650587.1:c.*90_*103del	ENSP00000497366.1:n.*90_*103del
ENST00000368786.5:c.*90_*103del	ENSP00000357775.1:n.*90_*103del
ENST00000368797.8:c.*90_*103del	ENSP00000357787.4:n.*90_*103del
ENST00000464267.1:n.985_998del
ENST00000465577.5:n.530_543del
ENST00000470483.1:n.576_589del
ENST00000484541.5:n.661_674del
ENST00000616800.4:c.161-3518_161-3505del
ENST00000622016.4:c.241-2939_241-2926del	ENSP00000483041.1:n.241-2939_241-2926del
NM_000375.2:c.*90_*103del	NP_000366.1:n.*90_*103del
XM_005270137.2:c.*90_*103del	XP_005270194.1:n.*90_*103del
XM_005270138.2:c.*90_*103del	XP_005270195.1:n.*90_*103del
XM_005270139.2:c.661-2939_661-2926del	XP_005270196.1:n.661-2939_661-2926del
XM_006717960.2:c.*90_*103del	XP_006718023.1:n.*90_*103del
XM_011540127.1:c.661-3518_661-3505del	XP_011538429.1:n.661-3518_661-3505del
XR_246103.2:n.1068_1081del
XR_945810.1:n.1298_1311del
NM_000375.3:c.*90_*103del MANE Select	NP_000366.1:n.*90_*103del
NM_001324036.1:c.*90_*103del	NP_001310965.1:n.*90_*103del
NM_001324037.1:c.*90_*103del	NP_001310966.1:n.*90_*103del
NM_001324038.1:c.*90_*103del	NP_001310967.1:n.*90_*103del
NR_136675.1:n.973_986del
NR_136676.1:n.1400_1413del
NR_136677.1:n.927-2939_927-2926del
NR_136678.1:n.884_897del
XM_011540127.2:c.661-3518_661-3505del	XP_011538429.1:n.661-3518_661-3505del
XM_017016611.2:c.*90_*103del	XP_016872100.2:n.*90_*103del
XM_017016612.2:c.661-2939_661-2926del	XP_016872101.1:n.661-2939_661-2926del
XM_024448154.1:c.*90_*103del	XP_024303922.1:n.*90_*103del
XR_002957010.1:n.2227_2240del
XR_246103.3:n.1083_1096del
XR_945810.2:n.1313_1326del
NM_001324036.2:c.*90_*103del	NP_001310965.1:n.*90_*103del
NM_001324037.2:c.*90_*103del	NP_001310966.1:n.*90_*103del
NM_001324038.2:c.*90_*103del	NP_001310967.1:n.*90_*103del
NR_136675.2:n.963_976del
NR_136676.2:n.1390_1403del
NR_136678.2:n.874_887del
NR_136677.2:n.917-2939_917-2926del