Canonical Allele Identifier: CA596582761

Gene: UROS

Linked Data

• dbSNP Id: rs1448010893
• gnomAD v2: 10-127477584-CAG-C
• gnomAD v3: 10-125789015-CAG-C
• gnomAD v4: 10-125789015-CAG-C
• MyVariant Identifiers: chr10:g.127477585_127477586del (hg19) ; chr10:g.125789016_125789017del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125789017_125789018del , CM000672.2:g.125789017_125789018del	GRCh38
NC_000010.10:g.127477586_127477587del , CM000672.1:g.127477586_127477587del	GRCh37
NC_000010.9:g.127467576_127467577del	NCBI36
NG_011557.1:g.39252_39253del
NG_011557.2:g.39252_39253del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.661-12_661-11del	ENSP00000518871.1:n.661-12_661-11del
ENST00000368797.10:c.661-12_661-11del MANE Select	ENSP00000357787.4:n.661-12_661-11del
ENST00000465577.6:c.681-12_681-11del
ENST00000648427.1:c.*659-12_*659-11del	ENSP00000497909.1:n.*659-12_*659-11del
ENST00000649536.1:c.661-12_661-11del	ENSP00000497817.1:n.661-12_661-11del
ENST00000650185.1:c.811-12_811-11del
ENST00000650472.1:n.3047-12_3047-11del
ENST00000650524.1:c.574-12_574-11del	ENSP00000498108.1:n.574-12_574-11del
ENST00000650587.1:c.742-12_742-11del	ENSP00000497366.1:n.742-12_742-11del
ENST00000368786.5:c.661-12_661-11del	ENSP00000357775.1:n.661-12_661-11del
ENST00000368797.8:c.661-12_661-11del	ENSP00000357787.4:n.661-12_661-11del
ENST00000464267.1:n.758-12_758-11del
ENST00000465577.5:n.303-12_303-11del
ENST00000470483.1:n.349-12_349-11del
ENST00000484541.5:n.434-12_434-11del
ENST00000616800.4:c.161-3757_161-3756del
ENST00000622016.4:c.241-3178_241-3177del	ENSP00000483041.1:n.241-3178_241-3177del
NM_000375.2:c.661-12_661-11del	NP_000366.1:n.661-12_661-11del
XM_005270137.2:c.742-12_742-11del	XP_005270194.1:n.742-12_742-11del
XM_005270138.2:c.661-12_661-11del	XP_005270195.1:n.661-12_661-11del
XM_005270139.2:c.661-3178_661-3177del	XP_005270196.1:n.661-3178_661-3177del
XM_006717960.2:c.742-12_742-11del	XP_006718023.1:n.742-12_742-11del
XM_011540127.1:c.661-3757_661-3756del	XP_011538429.1:n.661-3757_661-3756del
XR_246103.2:n.841-12_841-11del
XR_945810.1:n.1071-12_1071-11del
NM_000375.3:c.661-12_661-11del MANE Select	NP_000366.1:n.661-12_661-11del
NM_001324036.1:c.742-12_742-11del	NP_001310965.1:n.742-12_742-11del
NM_001324037.1:c.661-12_661-11del	NP_001310966.1:n.661-12_661-11del
NM_001324038.1:c.580-12_580-11del	NP_001310967.1:n.580-12_580-11del
NR_136675.1:n.746-12_746-11del
NR_136676.1:n.1173-12_1173-11del
NR_136677.1:n.927-3178_927-3177del
NR_136678.1:n.657-12_657-11del
XM_011540127.2:c.661-3757_661-3756del	XP_011538429.1:n.661-3757_661-3756del
XM_017016611.2:c.742-12_742-11del	XP_016872100.2:n.742-12_742-11del
XM_017016612.2:c.661-3178_661-3177del	XP_016872101.1:n.661-3178_661-3177del
XM_024448154.1:c.661-12_661-11del	XP_024303922.1:n.661-12_661-11del
XR_002957010.1:n.2000-12_2000-11del
XR_246103.3:n.856-12_856-11del
XR_945810.2:n.1086-12_1086-11del
NM_001324036.2:c.742-12_742-11del	NP_001310965.1:n.742-12_742-11del
NM_001324037.2:c.661-12_661-11del	NP_001310966.1:n.661-12_661-11del
NM_001324038.2:c.580-12_580-11del	NP_001310967.1:n.580-12_580-11del
NR_136675.2:n.736-12_736-11del
NR_136676.2:n.1163-12_1163-11del
NR_136678.2:n.647-12_647-11del
NR_136677.2:n.917-3178_917-3177del