Canonical Allele Identifier: CA2390794484

Gene: UBASH3A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42416025_42416027delinsCTG , CM000683.2:g.42416025_42416027delinsCTG	GRCh38
NC_000021.8:g.43836134_43836136delinsCTG , CM000683.1:g.43836134_43836136delinsCTG	GRCh37
NC_000021.7:g.42709203_42709205delinsCTG	NCBI36
NG_029750.1:g.17164_17166delinsCTG
NG_029750.2:g.17164_17166delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000319294.11:c.668-417_668-415delinsCTG MANE Select	ENSP00000317327.6:n.668-417_668-415delinsCTG
ENST00000291535.11:c.554-417_554-415delinsCTG	ENSP00000291535.6:n.554-417_554-415delinsCTG
ENST00000319294.10:c.668-417_668-415delinsCTG	ENSP00000317327.6:n.668-417_668-415delinsCTG
ENST00000398367.1:c.554-417_554-415delinsCTG	ENSP00000381408.1:n.554-417_554-415delinsCTG
ENST00000473381.1:c.554-417_554-415delinsCTG	ENSP00000489235.1:n.554-417_554-415delinsCTG
ENST00000635325.1:c.554-417_554-415delinsCTG	ENSP00000489463.1:n.554-417_554-415delinsCTG
NM_001001895.2:c.554-417_554-415delinsCTG	NP_001001895.1:n.554-417_554-415delinsCTG
NM_001243467.1:c.554-417_554-415delinsCTG	NP_001230396.1:n.554-417_554-415delinsCTG
NM_018961.3:c.668-417_668-415delinsCTG	NP_061834.1:n.668-417_668-415delinsCTG
XM_006724013.2:c.611-417_611-415delinsCTG	XP_006724076.1:n.611-417_611-415delinsCTG
XM_011529605.1:c.668-417_668-415delinsCTG	XP_011527907.1:n.668-417_668-415delinsCTG
XM_011529606.1:c.263-417_263-415delinsCTG	XP_011527908.1:n.263-417_263-415delinsCTG
XM_011529607.1:c.263-417_263-415delinsCTG	XP_011527909.1:n.263-417_263-415delinsCTG
XM_011529608.1:c.668-417_668-415delinsCTG	XP_011527910.1:n.668-417_668-415delinsCTG
XM_011529609.1:c.668-417_668-415delinsCTG	XP_011527911.1:n.668-417_668-415delinsCTG
XM_011529610.1:c.-433_-431delinsCTG	XP_011527912.1:n.-433_-431delinsCTG
XR_244316.1:n.638-417_638-415delinsCTG
XR_937510.1:n.638-417_638-415delinsCTG
XM_006724013.3:c.611-417_611-415delinsCTG	XP_006724076.1:n.611-417_611-415delinsCTG
XM_011529605.3:c.668-417_668-415delinsCTG	XP_011527907.1:n.668-417_668-415delinsCTG
XM_011529606.3:c.263-417_263-415delinsCTG	XP_011527908.1:n.263-417_263-415delinsCTG
XM_011529607.2:c.263-417_263-415delinsCTG	XP_011527909.1:n.263-417_263-415delinsCTG
XM_011529609.2:c.668-417_668-415delinsCTG	XP_011527911.1:n.668-417_668-415delinsCTG
XM_011529610.2:c.-433_-431delinsCTG	XP_011527912.1:n.-433_-431delinsCTG
XR_244316.2:n.620-417_620-415delinsCTG
NM_018961.4:c.668-417_668-415delinsCTG MANE Select	NP_061834.1:n.668-417_668-415delinsCTG
NM_001001895.3:c.554-417_554-415delinsCTG	NP_001001895.1:n.554-417_554-415delinsCTG
NM_001243467.2:c.554-417_554-415delinsCTG	NP_001230396.1:n.554-417_554-415delinsCTG