Canonical Allele Identifier: CA378687869

Gene: UROS

Linked Data

• MyVariant Identifiers: chr10:g.127486636T>A (hg19) ; chr10:g.125798067T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125798067T>A , CM000672.2:g.125798067T>A	GRCh38
NC_000010.10:g.127486636T>A , CM000672.1:g.127486636T>A	GRCh37
NC_000010.9:g.127476626T>A	NCBI36
NG_011557.1:g.30202A>T
NG_011557.2:g.30202A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.473A>T	ENSP00000518871.1:p.Lys158Ile
ENST00000368797.10:c.473A>T MANE Select	ENSP00000357787.4:p.Lys158Ile
ENST00000465577.6:c.150A>T
ENST00000648119.1:c.473A>T	ENSP00000497494.1:p.Lys158Ile
ENST00000648427.1:c.*128A>T	ENSP00000497909.1:n.*128A>T
ENST00000649275.1:c.402A>T
ENST00000649450.1:n.510A>T
ENST00000649536.1:c.395-1879A>T	ENSP00000497817.1:n.395-1879A>T
ENST00000650185.1:c.256A>T
ENST00000650472.1:n.2629A>T
ENST00000650524.1:c.314A>T	ENSP00000498108.1:n.314A>T
ENST00000650587.1:c.473A>T	ENSP00000497366.1:p.Lys158Ile
ENST00000368786.5:c.473A>T	ENSP00000357775.1:p.Lys158Ile
ENST00000368797.8:c.473A>T	ENSP00000357787.4:p.Lys158Ile
ENST00000420761.5:c.389A>T	ENSP00000414833.1:p.Lys130Ile
ENST00000462490.5:c.132A>T
ENST00000464267.1:n.37A>T
ENST00000465577.5:n.34A>T
ENST00000622016.4:c.53A>T	ENSP00000483041.1:p.Lys18Ile
NM_000375.2:c.473A>T	NP_000366.1:p.Lys158Ile
XM_005270137.2:c.473A>T	XP_005270194.1:p.Lys158Ile
XM_005270138.2:c.395-1879A>T	XP_005270195.1:n.395-1879A>T
XM_005270139.2:c.473A>T	XP_005270196.1:p.Lys158Ile
XM_005270140.3:c.473A>T	XP_005270197.1:p.Lys158Ile
XM_006717960.2:c.473A>T	XP_006718023.1:p.Lys158Ile
XM_011540126.1:c.473A>T	XP_011538428.1:p.Lys158Ile
XM_011540127.1:c.473A>T	XP_011538429.1:p.Lys158Ile
XR_246103.2:n.581A>T
XR_945809.1:n.581A>T
XR_945810.1:n.581A>T
NM_000375.3:c.473A>T MANE Select	NP_000366.1:p.Lys158Ile
NM_001324036.1:c.473A>T	NP_001310965.1:p.Lys158Ile
NM_001324037.1:c.395-1879A>T	NP_001310966.1:n.395-1879A>T
NM_001324038.1:c.395-1879A>T	NP_001310967.1:n.395-1879A>T
NR_136675.1:n.558A>T
NR_136676.1:n.739A>T
NR_136677.1:n.739A>T
NR_136678.1:n.469A>T
XM_005270140.5:c.473A>T	XP_005270197.1:p.Lys158Ile
XM_011540127.2:c.473A>T	XP_011538429.1:p.Lys158Ile
XM_017016611.2:c.473A>T	XP_016872100.2:p.Lys158Ile
XM_017016612.2:c.473A>T	XP_016872101.1:p.Lys158Ile
XM_024448154.1:c.473A>T	XP_024303922.1:p.Lys158Ile
XM_024448155.1:c.395-1879A>T	XP_024303923.1:n.395-1879A>T
XR_001747196.2:n.596A>T
XR_001747197.2:n.596A>T
XR_002957009.1:n.596A>T
XR_002957010.1:n.537A>T
XR_246103.3:n.596A>T
XR_945810.2:n.596A>T
NM_001324036.2:c.473A>T	NP_001310965.1:p.Lys158Ile
NM_001324037.2:c.395-1879A>T	NP_001310966.1:n.395-1879A>T
NM_001324038.2:c.395-1879A>T	NP_001310967.1:n.395-1879A>T
NR_136675.2:n.548A>T
NR_136676.2:n.729A>T
NR_136678.2:n.459A>T
NR_136677.2:n.729A>T