Canonical Allele Identifier: CA2285036035

Gene: IMPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.11987195T= , CM000680.2:g.11987195T=	GRCh38
NC_000018.9:g.11987194T= , CM000680.1:g.11987194T=	GRCh37
NC_000018.8:g.11977194T=	NCBI36
NG_028104.1:g.10740T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269159.8:c.96+5430T= MANE Select	ENSP00000269159.3:n.96+5430T=
ENST00000269159.7:c.96+5430T=	ENSP00000269159.3:n.96+5430T=
ENST00000383376.9:c.96+5430T=	ENSP00000372867.4:n.96+5430T=
ENST00000588752.5:n.181+5990T=
ENST00000588927.5:c.-464+5502T=	ENSP00000464767.1:n.-464+5502T=
ENST00000589238.5:c.-472+6065T=	ENSP00000465416.1:n.-472+6065T=
ENST00000590107.5:c.96+5430T=	ENSP00000466059.1:n.96+5430T=
ENST00000590138.1:c.96+5430T=	ENSP00000465938.1:n.96+5430T=
ENST00000625802.2:c.96+5430T=	ENSP00000486461.1:n.96+5430T=
NM_014214.2:c.96+5430T=	NP_055029.1:n.96+5430T=
XM_011525661.1:c.-399+5430T=	XP_011523963.1:n.-399+5430T=
XM_011525661.3:c.-399+5430T=	XP_011523963.1:n.-399+5430T=
NM_014214.3:c.96+5430T= MANE Select	NP_055029.1:n.96+5430T=