Canonical Allele Identifier: CA1943001278

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789015_125789017delinsCAG , CM000672.2:g.125789015_125789017delinsCAG	GRCh38
NC_000010.10:g.127477584_127477586delinsCAG , CM000672.1:g.127477584_127477586delinsCAG	GRCh37
NC_000010.9:g.127467574_127467576delinsCAG	NCBI36
NG_011557.1:g.39252_39254delinsCTG
NG_011557.2:g.39252_39254delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-12_661-10delinsCTG	ENSP00000518871.1:n.661-12_661-10delinsCTG
ENST00000368797.10:c.661-12_661-10delinsCTG MANE Select	ENSP00000357787.4:n.661-12_661-10delinsCTG
ENST00000465577.6:c.681-12_681-10delinsCTG
ENST00000648427.1:c.*659-12_*659-10delinsCTG	ENSP00000497909.1:n.*659-12_*659-10delinsCTG
ENST00000649536.1:c.661-12_661-10delinsCTG	ENSP00000497817.1:n.661-12_661-10delinsCTG
ENST00000650185.1:c.811-12_811-10delinsCTG
ENST00000650472.1:n.3047-12_3047-10delinsCTG
ENST00000650524.1:c.574-12_574-10delinsCTG	ENSP00000498108.1:n.574-12_574-10delinsCTG
ENST00000650587.1:c.742-12_742-10delinsCTG	ENSP00000497366.1:n.742-12_742-10delinsCTG
ENST00000368786.5:c.661-12_661-10delinsCTG	ENSP00000357775.1:n.661-12_661-10delinsCTG
ENST00000368797.8:c.661-12_661-10delinsCTG	ENSP00000357787.4:n.661-12_661-10delinsCTG
ENST00000464267.1:n.758-12_758-10delinsCTG
ENST00000465577.5:n.303-12_303-10delinsCTG
ENST00000470483.1:n.349-12_349-10delinsCTG
ENST00000484541.5:n.434-12_434-10delinsCTG
ENST00000616800.4:c.161-3757_161-3755delinsCTG
ENST00000622016.4:c.241-3178_241-3176delinsCTG	ENSP00000483041.1:n.241-3178_241-3176delinsCTG
NM_000375.2:c.661-12_661-10delinsCTG	NP_000366.1:n.661-12_661-10delinsCTG
XM_005270137.2:c.742-12_742-10delinsCTG	XP_005270194.1:n.742-12_742-10delinsCTG
XM_005270138.2:c.661-12_661-10delinsCTG	XP_005270195.1:n.661-12_661-10delinsCTG
XM_005270139.2:c.661-3178_661-3176delinsCTG	XP_005270196.1:n.661-3178_661-3176delinsCTG
XM_006717960.2:c.742-12_742-10delinsCTG	XP_006718023.1:n.742-12_742-10delinsCTG
XM_011540127.1:c.661-3757_661-3755delinsCTG	XP_011538429.1:n.661-3757_661-3755delinsCTG
XR_246103.2:n.841-12_841-10delinsCTG
XR_945810.1:n.1071-12_1071-10delinsCTG
NM_000375.3:c.661-12_661-10delinsCTG MANE Select	NP_000366.1:n.661-12_661-10delinsCTG
NM_001324036.1:c.742-12_742-10delinsCTG	NP_001310965.1:n.742-12_742-10delinsCTG
NM_001324037.1:c.661-12_661-10delinsCTG	NP_001310966.1:n.661-12_661-10delinsCTG
NM_001324038.1:c.580-12_580-10delinsCTG	NP_001310967.1:n.580-12_580-10delinsCTG
NR_136675.1:n.746-12_746-10delinsCTG
NR_136676.1:n.1173-12_1173-10delinsCTG
NR_136677.1:n.927-3178_927-3176delinsCTG
NR_136678.1:n.657-12_657-10delinsCTG
XM_011540127.2:c.661-3757_661-3755delinsCTG	XP_011538429.1:n.661-3757_661-3755delinsCTG
XM_017016611.2:c.742-12_742-10delinsCTG	XP_016872100.2:n.742-12_742-10delinsCTG
XM_017016612.2:c.661-3178_661-3176delinsCTG	XP_016872101.1:n.661-3178_661-3176delinsCTG
XM_024448154.1:c.661-12_661-10delinsCTG	XP_024303922.1:n.661-12_661-10delinsCTG
XR_002957010.1:n.2000-12_2000-10delinsCTG
XR_246103.3:n.856-12_856-10delinsCTG
XR_945810.2:n.1086-12_1086-10delinsCTG
NM_001324036.2:c.742-12_742-10delinsCTG	NP_001310965.1:n.742-12_742-10delinsCTG
NM_001324037.2:c.661-12_661-10delinsCTG	NP_001310966.1:n.661-12_661-10delinsCTG
NM_001324038.2:c.580-12_580-10delinsCTG	NP_001310967.1:n.580-12_580-10delinsCTG
NR_136675.2:n.736-12_736-10delinsCTG
NR_136676.2:n.1163-12_1163-10delinsCTG
NR_136678.2:n.647-12_647-10delinsCTG
NR_136677.2:n.917-3178_917-3176delinsCTG