Canonical Allele Identifier: CA1943001284

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789027_125789029delinsCAG , CM000672.2:g.125789027_125789029delinsCAG	GRCh38
NC_000010.10:g.127477596_127477598delinsCAG , CM000672.1:g.127477596_127477598delinsCAG	GRCh37
NC_000010.9:g.127467586_127467588delinsCAG	NCBI36
NG_011557.1:g.39240_39242delinsCTG
NG_011557.2:g.39240_39242delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-24_661-22delinsCTG	ENSP00000518871.1:n.661-24_661-22delinsCTG
ENST00000368797.10:c.661-24_661-22delinsCTG MANE Select	ENSP00000357787.4:n.661-24_661-22delinsCTG
ENST00000465577.6:c.681-24_681-22delinsCTG
ENST00000648427.1:c.*659-24_*659-22delinsCTG	ENSP00000497909.1:n.*659-24_*659-22delinsCTG
ENST00000649536.1:c.661-24_661-22delinsCTG	ENSP00000497817.1:n.661-24_661-22delinsCTG
ENST00000650185.1:c.811-24_811-22delinsCTG
ENST00000650472.1:n.3047-24_3047-22delinsCTG
ENST00000650524.1:c.574-24_574-22delinsCTG	ENSP00000498108.1:n.574-24_574-22delinsCTG
ENST00000650587.1:c.742-24_742-22delinsCTG	ENSP00000497366.1:n.742-24_742-22delinsCTG
ENST00000368786.5:c.661-24_661-22delinsCTG	ENSP00000357775.1:n.661-24_661-22delinsCTG
ENST00000368797.8:c.661-24_661-22delinsCTG	ENSP00000357787.4:n.661-24_661-22delinsCTG
ENST00000464267.1:n.758-24_758-22delinsCTG
ENST00000465577.5:n.303-24_303-22delinsCTG
ENST00000470483.1:n.349-24_349-22delinsCTG
ENST00000484541.5:n.434-24_434-22delinsCTG
ENST00000616800.4:c.161-3769_161-3767delinsCTG
ENST00000622016.4:c.241-3190_241-3188delinsCTG	ENSP00000483041.1:n.241-3190_241-3188delinsCTG
NM_000375.2:c.661-24_661-22delinsCTG	NP_000366.1:n.661-24_661-22delinsCTG
XM_005270137.2:c.742-24_742-22delinsCTG	XP_005270194.1:n.742-24_742-22delinsCTG
XM_005270138.2:c.661-24_661-22delinsCTG	XP_005270195.1:n.661-24_661-22delinsCTG
XM_005270139.2:c.661-3190_661-3188delinsCTG	XP_005270196.1:n.661-3190_661-3188delinsCTG
XM_006717960.2:c.742-24_742-22delinsCTG	XP_006718023.1:n.742-24_742-22delinsCTG
XM_011540127.1:c.661-3769_661-3767delinsCTG	XP_011538429.1:n.661-3769_661-3767delinsCTG
XR_246103.2:n.841-24_841-22delinsCTG
XR_945810.1:n.1071-24_1071-22delinsCTG
NM_000375.3:c.661-24_661-22delinsCTG MANE Select	NP_000366.1:n.661-24_661-22delinsCTG
NM_001324036.1:c.742-24_742-22delinsCTG	NP_001310965.1:n.742-24_742-22delinsCTG
NM_001324037.1:c.661-24_661-22delinsCTG	NP_001310966.1:n.661-24_661-22delinsCTG
NM_001324038.1:c.580-24_580-22delinsCTG	NP_001310967.1:n.580-24_580-22delinsCTG
NR_136675.1:n.746-24_746-22delinsCTG
NR_136676.1:n.1173-24_1173-22delinsCTG
NR_136677.1:n.927-3190_927-3188delinsCTG
NR_136678.1:n.657-24_657-22delinsCTG
XM_011540127.2:c.661-3769_661-3767delinsCTG	XP_011538429.1:n.661-3769_661-3767delinsCTG
XM_017016611.2:c.742-24_742-22delinsCTG	XP_016872100.2:n.742-24_742-22delinsCTG
XM_017016612.2:c.661-3190_661-3188delinsCTG	XP_016872101.1:n.661-3190_661-3188delinsCTG
XM_024448154.1:c.661-24_661-22delinsCTG	XP_024303922.1:n.661-24_661-22delinsCTG
XR_002957010.1:n.2000-24_2000-22delinsCTG
XR_246103.3:n.856-24_856-22delinsCTG
XR_945810.2:n.1086-24_1086-22delinsCTG
NM_001324036.2:c.742-24_742-22delinsCTG	NP_001310965.1:n.742-24_742-22delinsCTG
NM_001324037.2:c.661-24_661-22delinsCTG	NP_001310966.1:n.661-24_661-22delinsCTG
NM_001324038.2:c.580-24_580-22delinsCTG	NP_001310967.1:n.580-24_580-22delinsCTG
NR_136675.2:n.736-24_736-22delinsCTG
NR_136676.2:n.1163-24_1163-22delinsCTG
NR_136678.2:n.647-24_647-22delinsCTG
NR_136677.2:n.917-3190_917-3188delinsCTG