Canonical Allele Identifier: CA2123796869

Gene: PSME2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146238C= , CM000676.2:g.24146238C=	GRCh38
NC_000014.8:g.24615447C= , CM000676.1:g.24615447C=	GRCh37
NC_000014.7:g.23685287C=	NCBI36
NG_042234.1:g.4364C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.51G= MANE Select	ENSP00000216802.5:p.Val17=
ENST00000216802.9:c.51G=	ENSP00000216802.5:p.Val17=
ENST00000471700.6:n.49G=
ENST00000558273.5:c.51G=	ENSP00000453195.1:p.Val17=
ENST00000558931.5:n.728G=
ENST00000559056.5:c.-181G=	ENSP00000452940.1:n.-181G=
ENST00000559453.5:n.1G=
ENST00000559493.5:n.48G=
ENST00000559613.1:n.99G=
ENST00000560370.3:c.51G=	ENSP00000453161.1:p.Val17=
ENST00000560410.5:c.48+296G=	ENSP00000453487.1:n.48+296G=
ENST00000560592.5:n.91G=
ENST00000560788.1:n.66G=
ENST00000615264.4:c.51G=	ENSP00000484569.1:p.Val17=
ENST00000630027.1:c.51G=	ENSP00000485798.1:p.Val17=
NM_002818.2:c.51G=	NP_002809.2:p.Val17=
XM_006720213.1:c.-305G=	XP_006720276.1:n.-305G=
XM_006720213.2:c.-305G=	XP_006720276.1:n.-305G=
NM_002818.3:c.51G= MANE Select	NP_002809.2:p.Val17=