Canonical Allele Identifier: CA501201556

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909296G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831936G>A , CM000679.2:g.63831936G>A	GRCh38
NC_000017.10:g.61909296G>A , CM000679.1:g.61909296G>A	GRCh37
NC_000017.9:g.59263028G>A	NCBI36
NG_053004.1:g.16056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*385G>A	ENSP00000464347.2:n.*385G>A
ENST00000703608.1:c.*705G>A	ENSP00000515392.1:n.*705G>A
ENST00000703609.1:c.1107G>A	ENSP00000515393.1:p.Glu369=
ENST00000703610.1:c.*465G>A	ENSP00000515394.1:n.*465G>A
ENST00000310144.11:c.1188G>A MANE Select	ENSP00000310572.6:p.Glu396=
ENST00000310144.10:c.1188G>A	ENSP00000310572.6:p.Glu396=
ENST00000375812.8:c.1164G>A	ENSP00000364970.4:p.Glu388=
ENST00000578570.5:n.1598G>A
ENST00000579147.5:n.2503G>A
ENST00000580864.5:c.1164G>A	ENSP00000462495.1:p.Glu388=
ENST00000581882.5:c.1164G>A	ENSP00000463938.1:p.Glu388=
ENST00000584657.1:n.493G>A
ENST00000585242.5:c.*959G>A	ENSP00000463107.1:n.*959G>A
NM_001199163.1:c.1164G>A	NP_001186092.1:p.Glu388=
NM_002805.5:c.1188G>A	NP_002796.4:p.Glu396=
XM_006721980.1:c.1188G>A	XP_006722043.1:p.Glu396=
XR_934508.1:n.1277G>A
XM_024450840.1:c.1269G>A	XP_024306608.1:p.Glu423=
XM_024450841.1:c.1245G>A	XP_024306609.1:p.Glu415=
XR_934508.2:n.1264G>A
NM_002805.6:c.1188G>A MANE Select	NP_002796.4:p.Glu396=
NM_001199163.2:c.1164G>A	NP_001186092.1:p.Glu388=