Canonical Allele Identifier: CA2123796820

Gene: PSME2

Linked Data

• dbSNP Id: rs2038151506
• gnomAD v4: 14-24146145-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146145G>T , CM000676.2:g.24146145G>T	GRCh38
NC_000014.8:g.24615354G>T , CM000676.1:g.24615354G>T	GRCh37
NC_000014.7:g.23685194G>T	NCBI36
NG_042234.1:g.4271G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.81+63C>A MANE Select	ENSP00000216802.5:n.81+63C>A
ENST00000216802.9:c.81+63C>A	ENSP00000216802.5:n.81+63C>A
ENST00000471700.6:n.79+63C>A
ENST00000558273.5:c.81+63C>A	ENSP00000453195.1:n.81+63C>A
ENST00000558931.5:n.821C>A
ENST00000559056.5:c.-151+63C>A	ENSP00000452940.1:n.-151+63C>A
ENST00000559453.5:n.94C>A
ENST00000559493.5:n.78+63C>A
ENST00000559613.1:n.129+63C>A
ENST00000560370.3:c.81+63C>A	ENSP00000453161.1:n.81+63C>A
ENST00000560410.5:c.49-373C>A	ENSP00000453487.1:n.49-373C>A
ENST00000560592.5:n.121+63C>A
ENST00000560788.1:n.159C>A
ENST00000615264.4:c.81+63C>A	ENSP00000484569.1:n.81+63C>A
ENST00000630027.1:c.81+63C>A	ENSP00000485798.1:n.81+63C>A
NM_002818.2:c.81+63C>A	NP_002809.2:n.81+63C>A
XM_006720213.1:c.-275+63C>A	XP_006720276.1:n.-275+63C>A
XM_006720213.2:c.-275+63C>A	XP_006720276.1:n.-275+63C>A
NM_002818.3:c.81+63C>A MANE Select	NP_002809.2:n.81+63C>A