Canonical Allele Identifier: CA2611362215

Gene: UROS

Linked Data

• gnomAD v4: 10-125789009-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789011_125789012del , CM000672.2:g.125789011_125789012del	GRCh38
NC_000010.10:g.127477580_127477581del , CM000672.1:g.127477580_127477581del	GRCh37
NC_000010.9:g.127467570_127467571del	NCBI36
NG_011557.1:g.39258_39259del
NG_011557.2:g.39258_39259del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-6_661-5del	ENSP00000518871.1:n.661-6_661-5del
ENST00000368797.10:c.661-6_661-5del MANE Select	ENSP00000357787.4:n.661-6_661-5del
ENST00000465577.6:c.681-6_681-5del
ENST00000648427.1:c.*659-6_*659-5del	ENSP00000497909.1:n.*659-6_*659-5del
ENST00000649536.1:c.661-6_661-5del	ENSP00000497817.1:n.661-6_661-5del
ENST00000650185.1:c.811-6_811-5del
ENST00000650472.1:n.3047-6_3047-5del
ENST00000650524.1:c.574-6_574-5del	ENSP00000498108.1:n.574-6_574-5del
ENST00000650587.1:c.742-6_742-5del	ENSP00000497366.1:n.742-6_742-5del
ENST00000368786.5:c.661-6_661-5del	ENSP00000357775.1:n.661-6_661-5del
ENST00000368797.8:c.661-6_661-5del	ENSP00000357787.4:n.661-6_661-5del
ENST00000464267.1:n.758-6_758-5del
ENST00000465577.5:n.303-6_303-5del
ENST00000470483.1:n.349-6_349-5del
ENST00000484541.5:n.434-6_434-5del
ENST00000616800.4:c.161-3751_161-3750del
ENST00000622016.4:c.241-3172_241-3171del	ENSP00000483041.1:n.241-3172_241-3171del
NM_000375.2:c.661-6_661-5del	NP_000366.1:n.661-6_661-5del
XM_005270137.2:c.742-6_742-5del	XP_005270194.1:n.742-6_742-5del
XM_005270138.2:c.661-6_661-5del	XP_005270195.1:n.661-6_661-5del
XM_005270139.2:c.661-3172_661-3171del	XP_005270196.1:n.661-3172_661-3171del
XM_006717960.2:c.742-6_742-5del	XP_006718023.1:n.742-6_742-5del
XM_011540127.1:c.661-3751_661-3750del	XP_011538429.1:n.661-3751_661-3750del
XR_246103.2:n.841-6_841-5del
XR_945810.1:n.1071-6_1071-5del
NM_000375.3:c.661-6_661-5del MANE Select	NP_000366.1:n.661-6_661-5del
NM_001324036.1:c.742-6_742-5del	NP_001310965.1:n.742-6_742-5del
NM_001324037.1:c.661-6_661-5del	NP_001310966.1:n.661-6_661-5del
NM_001324038.1:c.580-6_580-5del	NP_001310967.1:n.580-6_580-5del
NR_136675.1:n.746-6_746-5del
NR_136676.1:n.1173-6_1173-5del
NR_136677.1:n.927-3172_927-3171del
NR_136678.1:n.657-6_657-5del
XM_011540127.2:c.661-3751_661-3750del	XP_011538429.1:n.661-3751_661-3750del
XM_017016611.2:c.742-6_742-5del	XP_016872100.2:n.742-6_742-5del
XM_017016612.2:c.661-3172_661-3171del	XP_016872101.1:n.661-3172_661-3171del
XM_024448154.1:c.661-6_661-5del	XP_024303922.1:n.661-6_661-5del
XR_002957010.1:n.2000-6_2000-5del
XR_246103.3:n.856-6_856-5del
XR_945810.2:n.1086-6_1086-5del
NM_001324036.2:c.742-6_742-5del	NP_001310965.1:n.742-6_742-5del
NM_001324037.2:c.661-6_661-5del	NP_001310966.1:n.661-6_661-5del
NM_001324038.2:c.580-6_580-5del	NP_001310967.1:n.580-6_580-5del
NR_136675.2:n.736-6_736-5del
NR_136676.2:n.1163-6_1163-5del
NR_136678.2:n.647-6_647-5del
NR_136677.2:n.917-3172_917-3171del