Canonical Allele Identifier: CA2285050226

Gene: IMPA2

Linked Data

• dbSNP Id: rs1907602069

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12017199_12017202del , CM000680.2:g.12017199_12017202del	GRCh38
NC_000018.9:g.12017198_12017201del , CM000680.1:g.12017198_12017201del	GRCh37
NC_000018.8:g.12007198_12007201del	NCBI36
NG_028104.1:g.40744_40747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269159.8:c.490+2826_490+2829del MANE Select	ENSP00000269159.3:n.490+2826_490+2829del
ENST00000269159.7:c.490+2826_490+2829del	ENSP00000269159.3:n.490+2826_490+2829del
ENST00000383376.9:c.*492-415_*492-412del	ENSP00000372867.4:n.*492-415_*492-412del
ENST00000586230.1:c.212+2826_212+2829del
ENST00000588167.1:n.243+2826_243+2829del
ENST00000588752.5:n.575+2826_575+2829del
ENST00000588927.5:c.-78+2826_-78+2829del	ENSP00000464767.1:n.-78+2826_-78+2829del
ENST00000589238.5:c.-78+2826_-78+2829del	ENSP00000465416.1:n.-78+2826_-78+2829del
ENST00000590107.5:c.*132+2826_*132+2829del	ENSP00000466059.1:n.*132+2826_*132+2829del
ENST00000590138.1:c.*93+2826_*93+2829del	ENSP00000465938.1:n.*93+2826_*93+2829del
NM_014214.2:c.490+2826_490+2829del	NP_055029.1:n.490+2826_490+2829del
XM_011525659.1:c.442+2826_442+2829del	XP_011523961.1:n.442+2826_442+2829del
XM_011525660.1:c.418+2826_418+2829del	XP_011523962.1:n.418+2826_418+2829del
XM_011525661.1:c.130+2826_130+2829del	XP_011523963.1:n.130+2826_130+2829del
XM_011525659.3:c.442+2826_442+2829del	XP_011523961.1:n.442+2826_442+2829del
XM_011525661.3:c.130+2826_130+2829del	XP_011523963.1:n.130+2826_130+2829del
NM_014214.3:c.490+2826_490+2829del MANE Select	NP_055029.1:n.490+2826_490+2829del