Canonical Allele Identifier: CA257871799

Gene: PSME2

Linked Data

• dbSNP Id: rs573167075
• MyVariant Identifiers: chr14:g.24615339G>A (hg19) ; chr14:g.24146130G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146130G>A , CM000676.2:g.24146130G>A	GRCh38
NC_000014.8:g.24615339G>A , CM000676.1:g.24615339G>A	GRCh37
NC_000014.7:g.23685179G>A	NCBI36
NG_042234.1:g.4256G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216802.10:c.81+78C>T MANE Select	ENSP00000216802.5:n.81+78C>T
ENST00000216802.9:c.81+78C>T	ENSP00000216802.5:n.81+78C>T
ENST00000471700.6:n.79+78C>T
ENST00000558273.5:c.81+78C>T	ENSP00000453195.1:n.81+78C>T
ENST00000558931.5:n.836C>T
ENST00000559056.5:c.-151+78C>T	ENSP00000452940.1:n.-151+78C>T
ENST00000559453.5:n.109C>T
ENST00000559493.5:n.78+78C>T
ENST00000559613.1:n.129+78C>T
ENST00000560370.3:c.81+78C>T	ENSP00000453161.1:n.81+78C>T
ENST00000560410.5:c.49-358C>T	ENSP00000453487.1:n.49-358C>T
ENST00000560592.5:n.121+78C>T
ENST00000560788.1:n.174C>T
ENST00000615264.4:c.81+78C>T	ENSP00000484569.1:n.81+78C>T
ENST00000630027.1:c.81+78C>T	ENSP00000485798.1:n.81+78C>T
NM_002818.2:c.81+78C>T	NP_002809.2:n.81+78C>T
XM_006720213.1:c.-275+78C>T	XP_006720276.1:n.-275+78C>T
XM_006720213.2:c.-275+78C>T	XP_006720276.1:n.-275+78C>T
NM_002818.3:c.81+78C>T MANE Select	NP_002809.2:n.81+78C>T