Canonical Allele Identifier: CA661166282

Gene: UROS

Linked Data

• dbSNP Id: rs1358001959
• gnomAD v3: 10-125789092-C-A
• gnomAD v4: 10-125789092-C-A
• MyVariant Identifiers: chr10:g.127477661C>A (hg19) ; chr10:g.125789092C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789092C>A , CM000672.2:g.125789092C>A	GRCh38
NC_000010.10:g.127477661C>A , CM000672.1:g.127477661C>A	GRCh37
NC_000010.9:g.127467651C>A	NCBI36
NG_011557.1:g.39177G>T
NG_011557.2:g.39177G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-87G>T	ENSP00000518871.1:n.661-87G>T
ENST00000368797.10:c.661-87G>T MANE Select	ENSP00000357787.4:n.661-87G>T
ENST00000465577.6:c.681-87G>T
ENST00000648427.1:c.*659-87G>T	ENSP00000497909.1:n.*659-87G>T
ENST00000649536.1:c.661-87G>T	ENSP00000497817.1:n.661-87G>T
ENST00000650185.1:c.811-87G>T
ENST00000650472.1:n.3047-87G>T
ENST00000650524.1:c.574-87G>T	ENSP00000498108.1:n.574-87G>T
ENST00000650587.1:c.742-87G>T	ENSP00000497366.1:n.742-87G>T
ENST00000368786.5:c.661-87G>T	ENSP00000357775.1:n.661-87G>T
ENST00000368797.8:c.661-87G>T	ENSP00000357787.4:n.661-87G>T
ENST00000464267.1:n.758-87G>T
ENST00000465577.5:n.303-87G>T
ENST00000470483.1:n.349-87G>T
ENST00000484541.5:n.434-87G>T
ENST00000616800.4:c.161-3832G>T
ENST00000622016.4:c.241-3253G>T	ENSP00000483041.1:n.241-3253G>T
NM_000375.2:c.661-87G>T	NP_000366.1:n.661-87G>T
XM_005270137.2:c.742-87G>T	XP_005270194.1:n.742-87G>T
XM_005270138.2:c.661-87G>T	XP_005270195.1:n.661-87G>T
XM_005270139.2:c.661-3253G>T	XP_005270196.1:n.661-3253G>T
XM_006717960.2:c.742-87G>T	XP_006718023.1:n.742-87G>T
XM_011540127.1:c.661-3832G>T	XP_011538429.1:n.661-3832G>T
XR_246103.2:n.841-87G>T
XR_945810.1:n.1071-87G>T
NM_000375.3:c.661-87G>T MANE Select	NP_000366.1:n.661-87G>T
NM_001324036.1:c.742-87G>T	NP_001310965.1:n.742-87G>T
NM_001324037.1:c.661-87G>T	NP_001310966.1:n.661-87G>T
NM_001324038.1:c.580-87G>T	NP_001310967.1:n.580-87G>T
NR_136675.1:n.746-87G>T
NR_136676.1:n.1173-87G>T
NR_136677.1:n.927-3253G>T
NR_136678.1:n.657-87G>T
XM_011540127.2:c.661-3832G>T	XP_011538429.1:n.661-3832G>T
XM_017016611.2:c.742-87G>T	XP_016872100.2:n.742-87G>T
XM_017016612.2:c.661-3253G>T	XP_016872101.1:n.661-3253G>T
XM_024448154.1:c.661-87G>T	XP_024303922.1:n.661-87G>T
XR_002957010.1:n.2000-87G>T
XR_246103.3:n.856-87G>T
XR_945810.2:n.1086-87G>T
NM_001324036.2:c.742-87G>T	NP_001310965.1:n.742-87G>T
NM_001324037.2:c.661-87G>T	NP_001310966.1:n.661-87G>T
NM_001324038.2:c.580-87G>T	NP_001310967.1:n.580-87G>T
NR_136675.2:n.736-87G>T
NR_136676.2:n.1163-87G>T
NR_136678.2:n.647-87G>T
NR_136677.2:n.917-3253G>T