Canonical Allele Identifier: CA389281022
Gene: PSME2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24146227C>A , CM000676.2:g.24146227C>A GRCh38
NC_000014.8:g.24615436C>A , CM000676.1:g.24615436C>A GRCh37
NC_000014.7:g.23685276C>A NCBI36
NG_042234.1:g.4353C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216802.10:c.62G>T MANE Select ENSP00000216802.5:p.Arg21Ile
ENST00000216802.9:c.62G>T ENSP00000216802.5:p.Arg21Ile
ENST00000471700.6:n.60G>T
ENST00000558273.5:c.62G>T ENSP00000453195.1:p.Arg21Ile
ENST00000558931.5:n.739G>T
ENST00000559056.5:c.-170G>T ENSP00000452940.1:n.-170G>T
ENST00000559453.5:n.12G>T
ENST00000559493.5:n.59G>T
ENST00000559613.1:n.110G>T
ENST00000560370.3:c.62G>T ENSP00000453161.1:p.Arg21Ile
ENST00000560410.5:c.48+307G>T ENSP00000453487.1:n.48+307G>T
ENST00000560592.5:n.102G>T
ENST00000560788.1:n.77G>T
ENST00000615264.4:c.62G>T ENSP00000484569.1:p.Arg21Ile
ENST00000630027.1:c.62G>T ENSP00000485798.1:p.Arg21Ile
NM_002818.2:c.62G>T NP_002809.2:p.Arg21Ile
XM_006720213.1:c.-294G>T XP_006720276.1:n.-294G>T
XM_006720213.2:c.-294G>T XP_006720276.1:n.-294G>T
NM_002818.3:c.62G>T MANE Select NP_002809.2:p.Arg21Ile