Canonical Allele Identifier: CA2390794462

Gene: UBASH3A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42415989T= , CM000683.2:g.42415989T=	GRCh38
NC_000021.8:g.43836098T= , CM000683.1:g.43836098T=	GRCh37
NC_000021.7:g.42709167T=	NCBI36
NG_029750.1:g.17128T=
NG_029750.2:g.17128T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000319294.11:c.668-453T= MANE Select	ENSP00000317327.6:n.668-453T=
ENST00000291535.11:c.554-453T=	ENSP00000291535.6:n.554-453T=
ENST00000319294.10:c.668-453T=	ENSP00000317327.6:n.668-453T=
ENST00000398367.1:c.554-453T=	ENSP00000381408.1:n.554-453T=
ENST00000473381.1:c.554-453T=	ENSP00000489235.1:n.554-453T=
ENST00000635325.1:c.554-453T=	ENSP00000489463.1:n.554-453T=
NM_001001895.2:c.554-453T=	NP_001001895.1:n.554-453T=
NM_001243467.1:c.554-453T=	NP_001230396.1:n.554-453T=
NM_018961.3:c.668-453T=	NP_061834.1:n.668-453T=
XM_006724013.2:c.611-453T=	XP_006724076.1:n.611-453T=
XM_011529605.1:c.668-453T=	XP_011527907.1:n.668-453T=
XM_011529606.1:c.263-453T=	XP_011527908.1:n.263-453T=
XM_011529607.1:c.263-453T=	XP_011527909.1:n.263-453T=
XM_011529608.1:c.668-453T=	XP_011527910.1:n.668-453T=
XM_011529609.1:c.668-453T=	XP_011527911.1:n.668-453T=
XM_011529610.1:c.-469T=	XP_011527912.1:n.-469T=
XR_244316.1:n.638-453T=
XR_937510.1:n.638-453T=
XM_006724013.3:c.611-453T=	XP_006724076.1:n.611-453T=
XM_011529605.3:c.668-453T=	XP_011527907.1:n.668-453T=
XM_011529606.3:c.263-453T=	XP_011527908.1:n.263-453T=
XM_011529607.2:c.263-453T=	XP_011527909.1:n.263-453T=
XM_011529609.2:c.668-453T=	XP_011527911.1:n.668-453T=
XM_011529610.2:c.-469T=	XP_011527912.1:n.-469T=
XR_244316.2:n.620-453T=
NM_018961.4:c.668-453T= MANE Select	NP_061834.1:n.668-453T=
NM_001001895.3:c.554-453T=	NP_001001895.1:n.554-453T=
NM_001243467.2:c.554-453T=	NP_001230396.1:n.554-453T=