Canonical Allele Identifier: CA485661968

Gene: PSME2

Linked Data

• MyVariant Identifiers: chr14:g.24615447C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.24146238C>T , CM000676.2:g.24146238C>T	GRCh38
NC_000014.8:g.24615447C>T , CM000676.1:g.24615447C>T	GRCh37
NC_000014.7:g.23685287C>T	NCBI36
NG_042234.1:g.4364C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216802.10:c.51G>A MANE Select	ENSP00000216802.5:p.Val17=
ENST00000216802.9:c.51G>A	ENSP00000216802.5:p.Val17=
ENST00000471700.6:n.49G>A
ENST00000558273.5:c.51G>A	ENSP00000453195.1:p.Val17=
ENST00000558931.5:n.728G>A
ENST00000559056.5:c.-181G>A	ENSP00000452940.1:n.-181G>A
ENST00000559453.5:n.1G>A
ENST00000559493.5:n.48G>A
ENST00000559613.1:n.99G>A
ENST00000560370.3:c.51G>A	ENSP00000453161.1:p.Val17=
ENST00000560410.5:c.48+296G>A	ENSP00000453487.1:n.48+296G>A
ENST00000560592.5:n.91G>A
ENST00000560788.1:n.66G>A
ENST00000615264.4:c.51G>A	ENSP00000484569.1:p.Val17=
ENST00000630027.1:c.51G>A	ENSP00000485798.1:p.Val17=
NM_002818.2:c.51G>A	NP_002809.2:p.Val17=
XM_006720213.1:c.-305G>A	XP_006720276.1:n.-305G>A
XM_006720213.2:c.-305G>A	XP_006720276.1:n.-305G>A
NM_002818.3:c.51G>A MANE Select	NP_002809.2:p.Val17=