Canonical Allele Identifier: CA2123796867

Gene: PSME2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146235C= , CM000676.2:g.24146235C=	GRCh38
NC_000014.8:g.24615444C= , CM000676.1:g.24615444C=	GRCh37
NC_000014.7:g.23685284C=	NCBI36
NG_042234.1:g.4361C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.54G= MANE Select	ENSP00000216802.5:p.Glu18=
ENST00000216802.9:c.54G=	ENSP00000216802.5:p.Glu18=
ENST00000471700.6:n.52G=
ENST00000558273.5:c.54G=	ENSP00000453195.1:p.Glu18=
ENST00000558931.5:n.731G=
ENST00000559056.5:c.-178G=	ENSP00000452940.1:n.-178G=
ENST00000559453.5:n.4G=
ENST00000559493.5:n.51G=
ENST00000559613.1:n.102G=
ENST00000560370.3:c.54G=	ENSP00000453161.1:p.Glu18=
ENST00000560410.5:c.48+299G=	ENSP00000453487.1:n.48+299G=
ENST00000560592.5:n.94G=
ENST00000560788.1:n.69G=
ENST00000615264.4:c.54G=	ENSP00000484569.1:p.Glu18=
ENST00000630027.1:c.54G=	ENSP00000485798.1:p.Glu18=
NM_002818.2:c.54G=	NP_002809.2:p.Glu18=
XM_006720213.1:c.-302G=	XP_006720276.1:n.-302G=
XM_006720213.2:c.-302G=	XP_006720276.1:n.-302G=
NM_002818.3:c.54G= MANE Select	NP_002809.2:p.Glu18=