Canonical Allele Identifier: CA400596559

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909282C>A (hg19) ; chr17:g.63831922C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831922C>A , CM000679.2:g.63831922C>A	GRCh38
NC_000017.10:g.61909282C>A , CM000679.1:g.61909282C>A	GRCh37
NC_000017.9:g.59263014C>A	NCBI36
NG_053004.1:g.16070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*371C>A	ENSP00000464347.2:n.*371C>A
ENST00000703608.1:c.*691C>A	ENSP00000515392.1:n.*691C>A
ENST00000703609.1:c.1093C>A	ENSP00000515393.1:p.Gln365Lys
ENST00000703610.1:c.*451C>A	ENSP00000515394.1:n.*451C>A
ENST00000310144.11:c.1174C>A MANE Select	ENSP00000310572.6:p.Gln392Lys
ENST00000310144.10:c.1174C>A	ENSP00000310572.6:p.Gln392Lys
ENST00000375812.8:c.1150C>A	ENSP00000364970.4:p.Gln384Lys
ENST00000578570.5:n.1584C>A
ENST00000579147.5:n.2489C>A
ENST00000580864.5:c.1150C>A	ENSP00000462495.1:p.Gln384Lys
ENST00000581882.5:c.1150C>A	ENSP00000463938.1:p.Gln384Lys
ENST00000584657.1:n.479C>A
ENST00000585242.5:c.*945C>A	ENSP00000463107.1:n.*945C>A
NM_001199163.1:c.1150C>A	NP_001186092.1:p.Gln384Lys
NM_002805.5:c.1174C>A	NP_002796.4:p.Gln392Lys
XM_006721980.1:c.1174C>A	XP_006722043.1:p.Gln392Lys
XR_934508.1:n.1263C>A
XM_024450840.1:c.1255C>A	XP_024306608.1:p.Gln419Lys
XM_024450841.1:c.1231C>A	XP_024306609.1:p.Gln411Lys
XR_934508.2:n.1250C>A
NM_002805.6:c.1174C>A MANE Select	NP_002796.4:p.Gln392Lys
NM_001199163.2:c.1150C>A	NP_001186092.1:p.Gln384Lys