Canonical Allele Identifier: CA2285036014

Gene: IMPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11987167C= , CM000680.2:g.11987167C=	GRCh38
NC_000018.9:g.11987166C= , CM000680.1:g.11987166C=	GRCh37
NC_000018.8:g.11977166C=	NCBI36
NG_028104.1:g.10712C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269159.8:c.96+5402C= MANE Select	ENSP00000269159.3:n.96+5402C=
ENST00000269159.7:c.96+5402C=	ENSP00000269159.3:n.96+5402C=
ENST00000383376.9:c.96+5402C=	ENSP00000372867.4:n.96+5402C=
ENST00000588752.5:n.181+5962C=
ENST00000588927.5:c.-464+5474C=	ENSP00000464767.1:n.-464+5474C=
ENST00000589238.5:c.-472+6037C=	ENSP00000465416.1:n.-472+6037C=
ENST00000590107.5:c.96+5402C=	ENSP00000466059.1:n.96+5402C=
ENST00000590138.1:c.96+5402C=	ENSP00000465938.1:n.96+5402C=
ENST00000625802.2:c.96+5402C=	ENSP00000486461.1:n.96+5402C=
NM_014214.2:c.96+5402C=	NP_055029.1:n.96+5402C=
XM_011525661.1:c.-399+5402C=	XP_011523963.1:n.-399+5402C=
XM_011525661.3:c.-399+5402C=	XP_011523963.1:n.-399+5402C=
NM_014214.3:c.96+5402C= MANE Select	NP_055029.1:n.96+5402C=