Canonical Allele Identifier: CA1943013915

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125823049_125823050delinsAC , CM000672.2:g.125823049_125823050delinsAC	GRCh38
NC_000010.10:g.127511618_127511619delinsAC , CM000672.1:g.127511618_127511619delinsAC	GRCh37
NC_000010.9:g.127501608_127501609delinsAC	NCBI36
NG_011557.1:g.5219_5220delinsGT
NG_029095.1:g.4515_4516delinsAC
NG_011557.2:g.5219_5220delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.-48_-47delinsGT	ENSP00000518871.1:n.-48_-47delinsGT
ENST00000368797.10:c.-48_-47delinsGT MANE Select	ENSP00000357787.4:n.-48_-47delinsGT
ENST00000648119.1:c.-48_-47delinsGT	ENSP00000497494.1:n.-48_-47delinsGT
ENST00000648427.1:c.-48_-47delinsGT	ENSP00000497909.1:n.-48_-47delinsGT
ENST00000649536.1:c.-48_-47delinsGT	ENSP00000497817.1:n.-48_-47delinsGT
ENST00000368774.1:c.-48_-47delinsGT	ENSP00000357763.1:n.-48_-47delinsGT
ENST00000368778.7:c.-48_-47delinsGT	ENSP00000357767.3:n.-48_-47delinsGT
ENST00000368797.8:c.-48_-47delinsGT	ENSP00000357787.4:n.-48_-47delinsGT
ENST00000420761.5:c.-48_-47delinsGT	ENSP00000414833.1:n.-48_-47delinsGT
NM_000375.2:c.-48_-47delinsGT	NP_000366.1:n.-48_-47delinsGT
XM_005270137.2:c.-48_-47delinsGT	XP_005270194.1:n.-48_-47delinsGT
XM_005270139.2:c.-48_-47delinsGT	XP_005270196.1:n.-48_-47delinsGT
XM_005270140.3:c.-48_-47delinsGT	XP_005270197.1:n.-48_-47delinsGT
XM_006717960.2:c.-27+157_-27+158delinsGT	XP_006718023.1:n.-27+157_-27+158delinsGT
XM_011540126.1:c.-48_-47delinsGT	XP_011538428.1:n.-48_-47delinsGT
XM_011540127.1:c.-48_-47delinsGT	XP_011538429.1:n.-48_-47delinsGT
XR_246103.2:n.61_62delinsGT
XR_945809.1:n.61_62delinsGT
XR_945810.1:n.61_62delinsGT
NM_000375.3:c.-48_-47delinsGT MANE Select	NP_000366.1:n.-48_-47delinsGT
NM_001324036.1:c.-48_-47delinsGT	NP_001310965.1:n.-48_-47delinsGT
NM_001324037.1:c.-48_-47delinsGT	NP_001310966.1:n.-48_-47delinsGT
NM_001324038.1:c.-48_-47delinsGT	NP_001310967.1:n.-48_-47delinsGT
NM_001324039.1:c.-48_-47delinsGT	NP_001310968.1:n.-48_-47delinsGT
NR_136675.1:n.219_220delinsGT
NR_136676.1:n.219_220delinsGT
NR_136677.1:n.219_220delinsGT
NR_136678.1:n.219_220delinsGT
XM_005270140.5:c.-48_-47delinsGT	XP_005270197.1:n.-48_-47delinsGT
XM_011540127.2:c.-48_-47delinsGT	XP_011538429.1:n.-48_-47delinsGT
XM_017016611.2:c.-27+157_-27+158delinsGT	XP_016872100.2:n.-27+157_-27+158delinsGT
XM_017016612.2:c.-48_-47delinsGT	XP_016872101.1:n.-48_-47delinsGT
XM_024448154.1:c.-27+157_-27+158delinsGT	XP_024303922.1:n.-27+157_-27+158delinsGT
XM_024448155.1:c.-48_-47delinsGT	XP_024303923.1:n.-48_-47delinsGT
XR_001747196.2:n.76_77delinsGT
XR_001747197.2:n.76_77delinsGT
XR_002957009.1:n.76_77delinsGT
XR_002957010.1:n.38+157_38+158delinsGT
XR_246103.3:n.76_77delinsGT
XR_945810.2:n.76_77delinsGT
NM_001324036.2:c.-48_-47delinsGT	NP_001310965.1:n.-48_-47delinsGT
NM_001324037.2:c.-48_-47delinsGT	NP_001310966.1:n.-48_-47delinsGT
NM_001324038.2:c.-48_-47delinsGT	NP_001310967.1:n.-48_-47delinsGT
NR_136675.2:n.209_210delinsGT
NR_136676.2:n.209_210delinsGT
NR_136678.2:n.209_210delinsGT
NM_001324039.2:c.-48_-47delinsGT	NP_001310968.1:n.-48_-47delinsGT
NR_136677.2:n.209_210delinsGT