Canonical Allele Identifier: CA215313039

Gene: UROS

Linked Data

• dbSNP Id: rs111242345
• gnomAD v4: 10-125823161-C-A
• MyVariant Identifiers: chr10:g.127511730C>A (hg19) ; chr10:g.125823161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125823161C>A , CM000672.2:g.125823161C>A	GRCh38
NC_000010.10:g.127511730C>A , CM000672.1:g.127511730C>A	GRCh37
NC_000010.9:g.127501720C>A	NCBI36
NG_011557.1:g.5108G>T
NG_029095.1:g.4627C>A
NG_011557.2:g.5108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.-159G>T	ENSP00000518871.1:n.-159G>T
ENST00000368797.10:c.-159G>T MANE Select	ENSP00000357787.4:n.-159G>T
ENST00000648119.1:c.-159G>T	ENSP00000497494.1:n.-159G>T
ENST00000648427.1:c.-159G>T	ENSP00000497909.1:n.-159G>T
ENST00000649536.1:c.-159G>T	ENSP00000497817.1:n.-159G>T
ENST00000368778.7:c.-159G>T	ENSP00000357767.3:n.-159G>T
ENST00000368797.8:c.-159G>T	ENSP00000357787.4:n.-159G>T
ENST00000420761.5:c.-159G>T	ENSP00000414833.1:n.-159G>T
NM_000375.2:c.-159G>T	NP_000366.1:n.-159G>T
XM_006717960.2:c.-27+46G>T	XP_006718023.1:n.-27+46G>T
NM_000375.3:c.-159G>T MANE Select	NP_000366.1:n.-159G>T
NM_001324036.1:c.-159G>T	NP_001310965.1:n.-159G>T
NM_001324037.1:c.-159G>T	NP_001310966.1:n.-159G>T
NM_001324038.1:c.-159G>T	NP_001310967.1:n.-159G>T
NM_001324039.1:c.-159G>T	NP_001310968.1:n.-159G>T
NR_136675.1:n.108G>T
NR_136676.1:n.108G>T
NR_136677.1:n.108G>T
NR_136678.1:n.108G>T
XM_017016611.2:c.-27+46G>T	XP_016872100.2:n.-27+46G>T
XM_024448154.1:c.-27+46G>T	XP_024303922.1:n.-27+46G>T
XM_024448155.1:c.-159G>T	XP_024303923.1:n.-159G>T
XR_002957010.1:n.38+46G>T
NM_001324036.2:c.-159G>T	NP_001310965.1:n.-159G>T
NM_001324037.2:c.-159G>T	NP_001310966.1:n.-159G>T
NM_001324038.2:c.-159G>T	NP_001310967.1:n.-159G>T
NR_136675.2:n.98G>T
NR_136676.2:n.98G>T
NR_136678.2:n.98G>T
NM_001324039.2:c.-159G>T	NP_001310968.1:n.-159G>T
NR_136677.2:n.98G>T