Canonical Allele Identifier: CA2123796880

Gene: PSME2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146248G= , CM000676.2:g.24146248G=	GRCh38
NC_000014.8:g.24615457G= , CM000676.1:g.24615457G=	GRCh37
NC_000014.7:g.23685297G=	NCBI36
NG_042234.1:g.4374G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216802.10:c.49-8C= MANE Select	ENSP00000216802.5:n.49-8C=
ENST00000216802.9:c.49-8C=	ENSP00000216802.5:n.49-8C=
ENST00000471700.6:n.47-8C=
ENST00000558273.5:c.49-8C=	ENSP00000453195.1:n.49-8C=
ENST00000558931.5:n.726-8C=
ENST00000559056.5:c.-191C=	ENSP00000452940.1:n.-191C=
ENST00000559493.5:n.46-8C=
ENST00000559613.1:n.97-8C=
ENST00000560370.3:c.49-8C=	ENSP00000453161.1:n.49-8C=
ENST00000560410.5:c.48+286C=	ENSP00000453487.1:n.48+286C=
ENST00000560592.5:n.89-8C=
ENST00000560788.1:n.64-8C=
ENST00000615264.4:c.49-8C=	ENSP00000484569.1:n.49-8C=
ENST00000630027.1:c.49-8C=	ENSP00000485798.1:n.49-8C=
NM_002818.2:c.49-8C=	NP_002809.2:n.49-8C=
XM_006720213.1:c.-307-8C=	XP_006720276.1:n.-307-8C=
XM_006720213.2:c.-307-8C=	XP_006720276.1:n.-307-8C=
NM_002818.3:c.49-8C= MANE Select	NP_002809.2:n.49-8C=