Canonical Allele Identifier: CA378685451

Gene: UROS

Linked Data

• MyVariant Identifiers: chr10:g.127477438C>G (hg19) ; chr10:g.125788869C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125788869C>G , CM000672.2:g.125788869C>G	GRCh38
NC_000010.10:g.127477438C>G , CM000672.1:g.127477438C>G	GRCh37
NC_000010.9:g.127467428C>G	NCBI36
NG_011557.1:g.39400G>C
NG_011557.2:g.39400G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.797G>C	ENSP00000518871.1:p.Ter266Ser
ENST00000368797.10:c.797G>C MANE Select	ENSP00000357787.4:p.Ter266Ser
ENST00000465577.6:c.817G>C
ENST00000648427.1:c.*795G>C	ENSP00000497909.1:n.*795G>C
ENST00000649536.1:c.797G>C	ENSP00000497817.1:p.Ter266Ser
ENST00000650472.1:n.3183G>C
ENST00000650524.1:c.710G>C	ENSP00000498108.1:n.710G>C
ENST00000650587.1:c.878G>C	ENSP00000497366.1:p.Ter293Ser
ENST00000368786.5:c.797G>C	ENSP00000357775.1:p.Ter266Ser
ENST00000368797.8:c.797G>C	ENSP00000357787.4:p.Ter266Ser
ENST00000464267.1:n.894G>C
ENST00000465577.5:n.439G>C
ENST00000470483.1:n.485G>C
ENST00000484541.5:n.570G>C
ENST00000616800.4:c.161-3609G>C
ENST00000622016.4:c.241-3030G>C	ENSP00000483041.1:n.241-3030G>C
NM_000375.2:c.797G>C	NP_000366.1:p.Ter266Ser
XM_005270137.2:c.878G>C	XP_005270194.1:p.Ter293Ser
XM_005270138.2:c.797G>C	XP_005270195.1:p.Ter266Ser
XM_005270139.2:c.661-3030G>C	XP_005270196.1:n.661-3030G>C
XM_006717960.2:c.878G>C	XP_006718023.1:p.Ter293Ser
XM_011540127.1:c.661-3609G>C	XP_011538429.1:n.661-3609G>C
XR_246103.2:n.977G>C
XR_945810.1:n.1207G>C
NM_000375.3:c.797G>C MANE Select	NP_000366.1:p.Ter266Ser
NM_001324036.1:c.878G>C	NP_001310965.1:p.Ter293Ser
NM_001324037.1:c.797G>C	NP_001310966.1:p.Ter266Ser
NM_001324038.1:c.716G>C	NP_001310967.1:p.Ter239Ser
NR_136675.1:n.882G>C
NR_136676.1:n.1309G>C
NR_136677.1:n.927-3030G>C
NR_136678.1:n.793G>C
XM_011540127.2:c.661-3609G>C	XP_011538429.1:n.661-3609G>C
XM_017016611.2:c.878G>C	XP_016872100.2:p.Ter293Ser
XM_017016612.2:c.661-3030G>C	XP_016872101.1:n.661-3030G>C
XM_024448154.1:c.797G>C	XP_024303922.1:p.Ter266Ser
XR_002957010.1:n.2136G>C
XR_246103.3:n.992G>C
XR_945810.2:n.1222G>C
NM_001324036.2:c.878G>C	NP_001310965.1:p.Ter293Ser
NM_001324037.2:c.797G>C	NP_001310966.1:p.Ter266Ser
NM_001324038.2:c.716G>C	NP_001310967.1:p.Ter239Ser
NR_136675.2:n.872G>C
NR_136676.2:n.1299G>C
NR_136678.2:n.783G>C
NR_136677.2:n.917-3030G>C