Canonical Allele Identifier: CA2123796864

Gene: PSME2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146233A= , CM000676.2:g.24146233A=	GRCh38
NC_000014.8:g.24615442A= , CM000676.1:g.24615442A=	GRCh37
NC_000014.7:g.23685282A=	NCBI36
NG_042234.1:g.4359A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.56T= MANE Select	ENSP00000216802.5:p.Val19=
ENST00000216802.9:c.56T=	ENSP00000216802.5:p.Val19=
ENST00000471700.6:n.54T=
ENST00000558273.5:c.56T=	ENSP00000453195.1:p.Val19=
ENST00000558931.5:n.733T=
ENST00000559056.5:c.-176T=	ENSP00000452940.1:n.-176T=
ENST00000559453.5:n.6T=
ENST00000559493.5:n.53T=
ENST00000559613.1:n.104T=
ENST00000560370.3:c.56T=	ENSP00000453161.1:p.Val19=
ENST00000560410.5:c.48+301T=	ENSP00000453487.1:n.48+301T=
ENST00000560592.5:n.96T=
ENST00000560788.1:n.71T=
ENST00000615264.4:c.56T=	ENSP00000484569.1:p.Val19=
ENST00000630027.1:c.56T=	ENSP00000485798.1:p.Val19=
NM_002818.2:c.56T=	NP_002809.2:p.Val19=
XM_006720213.1:c.-300T=	XP_006720276.1:n.-300T=
XM_006720213.2:c.-300T=	XP_006720276.1:n.-300T=
NM_002818.3:c.56T= MANE Select	NP_002809.2:p.Val19=