Canonical Allele Identifier: CA378660634

Gene: UROS

Linked Data

• gnomAD v4: 10-125812271-T-C
• MyVariant Identifiers: chr10:g.127500840T>C (hg19) ; chr10:g.125812271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125812271T>C , CM000672.2:g.125812271T>C	GRCh38
NC_000010.10:g.127500840T>C , CM000672.1:g.127500840T>C	GRCh37
NC_000010.9:g.127490830T>C	NCBI36
NG_011557.1:g.15998A>G
NG_011557.2:g.15998A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.262A>G	ENSP00000518871.1:p.Lys88Glu
ENST00000368797.10:c.262A>G MANE Select	ENSP00000357787.4:p.Lys88Glu
ENST00000648119.1:c.262A>G	ENSP00000497494.1:p.Lys88Glu
ENST00000648427.1:c.262A>G	ENSP00000497909.1:p.Lys88Glu
ENST00000649275.1:c.191A>G
ENST00000649450.1:n.299A>G
ENST00000649536.1:c.262A>G	ENSP00000497817.1:p.Lys88Glu
ENST00000650185.1:c.45A>G
ENST00000650524.1:c.67A>G	ENSP00000498108.1:p.Lys23Glu
ENST00000650587.1:c.262A>G	ENSP00000497366.1:p.Lys88Glu
ENST00000368774.1:c.262A>G	ENSP00000357763.1:p.Lys88Glu
ENST00000368778.7:c.262A>G	ENSP00000357767.3:p.Lys88Glu
ENST00000368786.5:c.262A>G	ENSP00000357775.1:p.Lys88Glu
ENST00000368797.8:c.262A>G	ENSP00000357787.4:p.Lys88Glu
ENST00000420761.5:c.178A>G	ENSP00000414833.1:p.Lys60Glu
NM_000375.2:c.262A>G	NP_000366.1:p.Lys88Glu
XM_005270137.2:c.262A>G	XP_005270194.1:p.Lys88Glu
XM_005270138.2:c.262A>G	XP_005270195.1:p.Lys88Glu
XM_005270139.2:c.262A>G	XP_005270196.1:p.Lys88Glu
XM_005270140.3:c.262A>G	XP_005270197.1:p.Lys88Glu
XM_005270141.1:c.262A>G	XP_005270198.1:p.Lys88Glu
XM_006717960.2:c.262A>G	XP_006718023.1:p.Lys88Glu
XM_011540126.1:c.262A>G	XP_011538428.1:p.Lys88Glu
XM_011540127.1:c.262A>G	XP_011538429.1:p.Lys88Glu
XR_246103.2:n.370A>G
XR_945809.1:n.370A>G
XR_945810.1:n.370A>G
NM_000375.3:c.262A>G MANE Select	NP_000366.1:p.Lys88Glu
NM_001324036.1:c.262A>G	NP_001310965.1:p.Lys88Glu
NM_001324037.1:c.262A>G	NP_001310966.1:p.Lys88Glu
NM_001324038.1:c.262A>G	NP_001310967.1:p.Lys88Glu
NM_001324039.1:c.262A>G	NP_001310968.1:p.Lys88Glu
NR_136675.1:n.347A>G
NR_136676.1:n.528A>G
NR_136677.1:n.528A>G
NR_136678.1:n.258A>G
XM_005270140.5:c.262A>G	XP_005270197.1:p.Lys88Glu
XM_011540127.2:c.262A>G	XP_011538429.1:p.Lys88Glu
XM_017016611.2:c.262A>G	XP_016872100.2:p.Lys88Glu
XM_017016612.2:c.262A>G	XP_016872101.1:p.Lys88Glu
XM_024448154.1:c.262A>G	XP_024303922.1:p.Lys88Glu
XM_024448155.1:c.262A>G	XP_024303923.1:p.Lys88Glu
XR_001747196.2:n.385A>G
XR_001747197.2:n.385A>G
XR_002957009.1:n.385A>G
XR_002957010.1:n.326A>G
XR_246103.3:n.385A>G
XR_945810.2:n.385A>G
NM_001324036.2:c.262A>G	NP_001310965.1:p.Lys88Glu
NM_001324037.2:c.262A>G	NP_001310966.1:p.Lys88Glu
NM_001324038.2:c.262A>G	NP_001310967.1:p.Lys88Glu
NR_136675.2:n.337A>G
NR_136676.2:n.518A>G
NR_136678.2:n.248A>G
NM_001324039.2:c.262A>G	NP_001310968.1:p.Lys88Glu
NR_136677.2:n.518A>G