Canonical Allele Identifier: CA2611362211

Gene: UROS

Linked Data

• gnomAD v4: 10-125789006-C-CTA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789009_125789010dup , CM000672.2:g.125789009_125789010dup	GRCh38
NC_000010.10:g.127477578_127477579dup , CM000672.1:g.127477578_127477579dup	GRCh37
NC_000010.9:g.127467568_127467569dup	NCBI36
NG_011557.1:g.39261_39262dup
NG_011557.2:g.39261_39262dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-3_661-2dup	ENSP00000518871.1:n.661-3_661-2dup
ENST00000368797.10:c.661-3_661-2dup MANE Select	ENSP00000357787.4:n.661-3_661-2dup
ENST00000465577.6:c.681-3_681-2dup
ENST00000648427.1:c.*659-3_*659-2dup	ENSP00000497909.1:n.*659-3_*659-2dup
ENST00000649536.1:c.661-3_661-2dup	ENSP00000497817.1:n.661-3_661-2dup
ENST00000650185.1:c.811-3_811-2dup
ENST00000650472.1:n.3047-3_3047-2dup
ENST00000650524.1:c.574-3_574-2dup	ENSP00000498108.1:n.574-3_574-2dup
ENST00000650587.1:c.742-3_742-2dup	ENSP00000497366.1:n.742-3_742-2dup
ENST00000368786.5:c.661-3_661-2dup	ENSP00000357775.1:n.661-3_661-2dup
ENST00000368797.8:c.661-3_661-2dup	ENSP00000357787.4:n.661-3_661-2dup
ENST00000464267.1:n.758-3_758-2dup
ENST00000465577.5:n.303-3_303-2dup
ENST00000470483.1:n.349-3_349-2dup
ENST00000484541.5:n.434-3_434-2dup
ENST00000616800.4:c.161-3748_161-3747dup
ENST00000622016.4:c.241-3169_241-3168dup	ENSP00000483041.1:n.241-3169_241-3168dup
NM_000375.2:c.661-3_661-2dup	NP_000366.1:n.661-3_661-2dup
XM_005270137.2:c.742-3_742-2dup	XP_005270194.1:n.742-3_742-2dup
XM_005270138.2:c.661-3_661-2dup	XP_005270195.1:n.661-3_661-2dup
XM_005270139.2:c.661-3169_661-3168dup	XP_005270196.1:n.661-3169_661-3168dup
XM_006717960.2:c.742-3_742-2dup	XP_006718023.1:n.742-3_742-2dup
XM_011540127.1:c.661-3748_661-3747dup	XP_011538429.1:n.661-3748_661-3747dup
XR_246103.2:n.841-3_841-2dup
XR_945810.1:n.1071-3_1071-2dup
NM_000375.3:c.661-3_661-2dup MANE Select	NP_000366.1:n.661-3_661-2dup
NM_001324036.1:c.742-3_742-2dup	NP_001310965.1:n.742-3_742-2dup
NM_001324037.1:c.661-3_661-2dup	NP_001310966.1:n.661-3_661-2dup
NM_001324038.1:c.580-3_580-2dup	NP_001310967.1:n.580-3_580-2dup
NR_136675.1:n.746-3_746-2dup
NR_136676.1:n.1173-3_1173-2dup
NR_136677.1:n.927-3169_927-3168dup
NR_136678.1:n.657-3_657-2dup
XM_011540127.2:c.661-3748_661-3747dup	XP_011538429.1:n.661-3748_661-3747dup
XM_017016611.2:c.742-3_742-2dup	XP_016872100.2:n.742-3_742-2dup
XM_017016612.2:c.661-3169_661-3168dup	XP_016872101.1:n.661-3169_661-3168dup
XM_024448154.1:c.661-3_661-2dup	XP_024303922.1:n.661-3_661-2dup
XR_002957010.1:n.2000-3_2000-2dup
XR_246103.3:n.856-3_856-2dup
XR_945810.2:n.1086-3_1086-2dup
NM_001324036.2:c.742-3_742-2dup	NP_001310965.1:n.742-3_742-2dup
NM_001324037.2:c.661-3_661-2dup	NP_001310966.1:n.661-3_661-2dup
NM_001324038.2:c.580-3_580-2dup	NP_001310967.1:n.580-3_580-2dup
NR_136675.2:n.736-3_736-2dup
NR_136676.2:n.1163-3_1163-2dup
NR_136678.2:n.647-3_647-2dup
NR_136677.2:n.917-3169_917-3168dup