Canonical Allele Identifier: CA2575491634

Gene: PSME2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146174T>G , CM000676.2:g.24146174T>G	GRCh38
NC_000014.8:g.24615383T>G , CM000676.1:g.24615383T>G	GRCh37
NC_000014.7:g.23685223T>G	NCBI36
NG_042234.1:g.4300T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.81+34A>C MANE Select	ENSP00000216802.5:n.81+34A>C
ENST00000216802.9:c.81+34A>C	ENSP00000216802.5:n.81+34A>C
ENST00000471700.6:n.79+34A>C
ENST00000558273.5:c.81+34A>C	ENSP00000453195.1:n.81+34A>C
ENST00000558931.5:n.792A>C
ENST00000559056.5:c.-151+34A>C	ENSP00000452940.1:n.-151+34A>C
ENST00000559453.5:n.65A>C
ENST00000559493.5:n.78+34A>C
ENST00000559613.1:n.129+34A>C
ENST00000560370.3:c.81+34A>C	ENSP00000453161.1:n.81+34A>C
ENST00000560410.5:c.48+360A>C	ENSP00000453487.1:n.48+360A>C
ENST00000560592.5:n.121+34A>C
ENST00000560788.1:n.130A>C
ENST00000615264.4:c.81+34A>C	ENSP00000484569.1:n.81+34A>C
ENST00000630027.1:c.81+34A>C	ENSP00000485798.1:n.81+34A>C
NM_002818.2:c.81+34A>C	NP_002809.2:n.81+34A>C
XM_006720213.1:c.-275+34A>C	XP_006720276.1:n.-275+34A>C
XM_006720213.2:c.-275+34A>C	XP_006720276.1:n.-275+34A>C
NM_002818.3:c.81+34A>C MANE Select	NP_002809.2:n.81+34A>C