Canonical Allele Identifier: CA2285050237

Gene: IMPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12017228_12017229delinsGC , CM000680.2:g.12017228_12017229delinsGC	GRCh38
NC_000018.9:g.12017227_12017228delinsGC , CM000680.1:g.12017227_12017228delinsGC	GRCh37
NC_000018.8:g.12007227_12007228delinsGC	NCBI36
NG_028104.1:g.40773_40774delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269159.8:c.490+2855_490+2856delinsGC MANE Select	ENSP00000269159.3:n.490+2855_490+2856delinsGC
ENST00000269159.7:c.490+2855_490+2856delinsGC	ENSP00000269159.3:n.490+2855_490+2856delinsGC
ENST00000383376.9:c.*492-386_*492-385delinsGC	ENSP00000372867.4:n.*492-386_*492-385delinsGC
ENST00000586230.1:c.212+2855_212+2856delinsGC
ENST00000588167.1:n.243+2855_243+2856delinsGC
ENST00000588752.5:n.575+2855_575+2856delinsGC
ENST00000588927.5:c.-78+2855_-78+2856delinsGC	ENSP00000464767.1:n.-78+2855_-78+2856delinsGC
ENST00000589238.5:c.-78+2855_-78+2856delinsGC	ENSP00000465416.1:n.-78+2855_-78+2856delinsGC
ENST00000590107.5:c.*132+2855_*132+2856delinsGC	ENSP00000466059.1:n.*132+2855_*132+2856delinsGC
ENST00000590138.1:c.*93+2855_*93+2856delinsGC	ENSP00000465938.1:n.*93+2855_*93+2856delinsGC
NM_014214.2:c.490+2855_490+2856delinsGC	NP_055029.1:n.490+2855_490+2856delinsGC
XM_011525659.1:c.442+2855_442+2856delinsGC	XP_011523961.1:n.442+2855_442+2856delinsGC
XM_011525660.1:c.418+2855_418+2856delinsGC	XP_011523962.1:n.418+2855_418+2856delinsGC
XM_011525661.1:c.130+2855_130+2856delinsGC	XP_011523963.1:n.130+2855_130+2856delinsGC
XM_011525659.3:c.442+2855_442+2856delinsGC	XP_011523961.1:n.442+2855_442+2856delinsGC
XM_011525661.3:c.130+2855_130+2856delinsGC	XP_011523963.1:n.130+2855_130+2856delinsGC
NM_014214.3:c.490+2855_490+2856delinsGC MANE Select	NP_055029.1:n.490+2855_490+2856delinsGC