Canonical Allele Identifier: CA2611362243

Gene: UROS

Linked Data

• gnomAD v4: 10-125789045-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789047_125789048dup , CM000672.2:g.125789047_125789048dup	GRCh38
NC_000010.10:g.127477616_127477617dup , CM000672.1:g.127477616_127477617dup	GRCh37
NC_000010.9:g.127467606_127467607dup	NCBI36
NG_011557.1:g.39222_39223dup
NG_011557.2:g.39222_39223dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-42_661-41dup	ENSP00000518871.1:n.661-42_661-41dup
ENST00000368797.10:c.661-42_661-41dup MANE Select	ENSP00000357787.4:n.661-42_661-41dup
ENST00000465577.6:c.681-42_681-41dup
ENST00000648427.1:c.*659-42_*659-41dup	ENSP00000497909.1:n.*659-42_*659-41dup
ENST00000649536.1:c.661-42_661-41dup	ENSP00000497817.1:n.661-42_661-41dup
ENST00000650185.1:c.811-42_811-41dup
ENST00000650472.1:n.3047-42_3047-41dup
ENST00000650524.1:c.574-42_574-41dup	ENSP00000498108.1:n.574-42_574-41dup
ENST00000650587.1:c.742-42_742-41dup	ENSP00000497366.1:n.742-42_742-41dup
ENST00000368786.5:c.661-42_661-41dup	ENSP00000357775.1:n.661-42_661-41dup
ENST00000368797.8:c.661-42_661-41dup	ENSP00000357787.4:n.661-42_661-41dup
ENST00000464267.1:n.758-42_758-41dup
ENST00000465577.5:n.303-42_303-41dup
ENST00000470483.1:n.349-42_349-41dup
ENST00000484541.5:n.434-42_434-41dup
ENST00000616800.4:c.161-3787_161-3786dup
ENST00000622016.4:c.241-3208_241-3207dup	ENSP00000483041.1:n.241-3208_241-3207dup
NM_000375.2:c.661-42_661-41dup	NP_000366.1:n.661-42_661-41dup
XM_005270137.2:c.742-42_742-41dup	XP_005270194.1:n.742-42_742-41dup
XM_005270138.2:c.661-42_661-41dup	XP_005270195.1:n.661-42_661-41dup
XM_005270139.2:c.661-3208_661-3207dup	XP_005270196.1:n.661-3208_661-3207dup
XM_006717960.2:c.742-42_742-41dup	XP_006718023.1:n.742-42_742-41dup
XM_011540127.1:c.661-3787_661-3786dup	XP_011538429.1:n.661-3787_661-3786dup
XR_246103.2:n.841-42_841-41dup
XR_945810.1:n.1071-42_1071-41dup
NM_000375.3:c.661-42_661-41dup MANE Select	NP_000366.1:n.661-42_661-41dup
NM_001324036.1:c.742-42_742-41dup	NP_001310965.1:n.742-42_742-41dup
NM_001324037.1:c.661-42_661-41dup	NP_001310966.1:n.661-42_661-41dup
NM_001324038.1:c.580-42_580-41dup	NP_001310967.1:n.580-42_580-41dup
NR_136675.1:n.746-42_746-41dup
NR_136676.1:n.1173-42_1173-41dup
NR_136677.1:n.927-3208_927-3207dup
NR_136678.1:n.657-42_657-41dup
XM_011540127.2:c.661-3787_661-3786dup	XP_011538429.1:n.661-3787_661-3786dup
XM_017016611.2:c.742-42_742-41dup	XP_016872100.2:n.742-42_742-41dup
XM_017016612.2:c.661-3208_661-3207dup	XP_016872101.1:n.661-3208_661-3207dup
XM_024448154.1:c.661-42_661-41dup	XP_024303922.1:n.661-42_661-41dup
XR_002957010.1:n.2000-42_2000-41dup
XR_246103.3:n.856-42_856-41dup
XR_945810.2:n.1086-42_1086-41dup
NM_001324036.2:c.742-42_742-41dup	NP_001310965.1:n.742-42_742-41dup
NM_001324037.2:c.661-42_661-41dup	NP_001310966.1:n.661-42_661-41dup
NM_001324038.2:c.580-42_580-41dup	NP_001310967.1:n.580-42_580-41dup
NR_136675.2:n.736-42_736-41dup
NR_136676.2:n.1163-42_1163-41dup
NR_136678.2:n.647-42_647-41dup
NR_136677.2:n.917-3208_917-3207dup