Canonical Allele Identifier: CA389281085

Gene: PSME2

Linked Data

• MyVariant Identifiers: chr14:g.24615442A>C (hg19) ; chr14:g.24146233A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.56T>G MANE Select	ENSP00000216802.5:p.Val19Gly
ENST00000216802.9:c.56T>G	ENSP00000216802.5:p.Val19Gly
ENST00000471700.6:n.54T>G
ENST00000558273.5:c.56T>G	ENSP00000453195.1:p.Val19Gly
ENST00000558931.5:n.733T>G
ENST00000559056.5:c.-176T>G	ENSP00000452940.1:n.-176T>G
ENST00000559453.5:n.6T>G
ENST00000559493.5:n.53T>G
ENST00000559613.1:n.104T>G
ENST00000560370.3:c.56T>G	ENSP00000453161.1:p.Val19Gly
ENST00000560410.5:c.48+301T>G	ENSP00000453487.1:n.48+301T>G
ENST00000560592.5:n.96T>G
ENST00000560788.1:n.71T>G
ENST00000615264.4:c.56T>G	ENSP00000484569.1:p.Val19Gly
ENST00000630027.1:c.56T>G	ENSP00000485798.1:p.Val19Gly
NM_002818.2:c.56T>G	NP_002809.2:p.Val19Gly
XM_006720213.1:c.-300T>G	XP_006720276.1:n.-300T>G
XM_006720213.2:c.-300T>G	XP_006720276.1:n.-300T>G
NM_002818.3:c.56T>G MANE Select	NP_002809.2:p.Val19Gly