Canonical Allele Identifier: CA378685740

Gene: UROS

Linked Data

• MyVariant Identifiers: chr10:g.127477510G>C (hg19) ; chr10:g.125788941G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125788941G>C , CM000672.2:g.125788941G>C	GRCh38
NC_000010.10:g.127477510G>C , CM000672.1:g.127477510G>C	GRCh37
NC_000010.9:g.127467500G>C	NCBI36
NG_011557.1:g.39328C>G
NG_011557.2:g.39328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.725C>G	ENSP00000518871.1:p.Thr242Ser
ENST00000368797.10:c.725C>G MANE Select	ENSP00000357787.4:p.Thr242Ser
ENST00000465577.6:c.745C>G
ENST00000648427.1:c.*723C>G	ENSP00000497909.1:n.*723C>G
ENST00000649536.1:c.725C>G	ENSP00000497817.1:p.Thr242Ser
ENST00000650185.1:c.875C>G
ENST00000650472.1:n.3111C>G
ENST00000650524.1:c.638C>G	ENSP00000498108.1:n.638C>G
ENST00000650587.1:c.806C>G	ENSP00000497366.1:p.Thr269Ser
ENST00000368786.5:c.725C>G	ENSP00000357775.1:p.Thr242Ser
ENST00000368797.8:c.725C>G	ENSP00000357787.4:p.Thr242Ser
ENST00000464267.1:n.822C>G
ENST00000465577.5:n.367C>G
ENST00000470483.1:n.413C>G
ENST00000484541.5:n.498C>G
ENST00000616800.4:c.161-3681C>G
ENST00000622016.4:c.241-3102C>G	ENSP00000483041.1:n.241-3102C>G
NM_000375.2:c.725C>G	NP_000366.1:p.Thr242Ser
XM_005270137.2:c.806C>G	XP_005270194.1:p.Thr269Ser
XM_005270138.2:c.725C>G	XP_005270195.1:p.Thr242Ser
XM_005270139.2:c.661-3102C>G	XP_005270196.1:n.661-3102C>G
XM_006717960.2:c.806C>G	XP_006718023.1:p.Thr269Ser
XM_011540127.1:c.661-3681C>G	XP_011538429.1:n.661-3681C>G
XR_246103.2:n.905C>G
XR_945810.1:n.1135C>G
NM_000375.3:c.725C>G MANE Select	NP_000366.1:p.Thr242Ser
NM_001324036.1:c.806C>G	NP_001310965.1:p.Thr269Ser
NM_001324037.1:c.725C>G	NP_001310966.1:p.Thr242Ser
NM_001324038.1:c.644C>G	NP_001310967.1:p.Thr215Ser
NR_136675.1:n.810C>G
NR_136676.1:n.1237C>G
NR_136677.1:n.927-3102C>G
NR_136678.1:n.721C>G
XM_011540127.2:c.661-3681C>G	XP_011538429.1:n.661-3681C>G
XM_017016611.2:c.806C>G	XP_016872100.2:p.Thr269Ser
XM_017016612.2:c.661-3102C>G	XP_016872101.1:n.661-3102C>G
XM_024448154.1:c.725C>G	XP_024303922.1:p.Thr242Ser
XR_002957010.1:n.2064C>G
XR_246103.3:n.920C>G
XR_945810.2:n.1150C>G
NM_001324036.2:c.806C>G	NP_001310965.1:p.Thr269Ser
NM_001324037.2:c.725C>G	NP_001310966.1:p.Thr242Ser
NM_001324038.2:c.644C>G	NP_001310967.1:p.Thr215Ser
NR_136675.2:n.800C>G
NR_136676.2:n.1227C>G
NR_136678.2:n.711C>G
NR_136677.2:n.917-3102C>G