Canonical Allele Identifier: CA501201561

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909308C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831948C>A , CM000679.2:g.63831948C>A	GRCh38
NC_000017.10:g.61909308C>A , CM000679.1:g.61909308C>A	GRCh37
NC_000017.9:g.59263040C>A	NCBI36
NG_053004.1:g.16044G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*397C>A	ENSP00000464347.2:n.*397C>A
ENST00000703608.1:c.*717C>A	ENSP00000515392.1:n.*717C>A
ENST00000703609.1:c.1119C>A	ENSP00000515393.1:p.Ser373=
ENST00000703610.1:c.*477C>A	ENSP00000515394.1:n.*477C>A
ENST00000310144.11:c.1200C>A MANE Select	ENSP00000310572.6:p.Ser400=
ENST00000310144.10:c.1200C>A	ENSP00000310572.6:p.Ser400=
ENST00000375812.8:c.1176C>A	ENSP00000364970.4:p.Ser392=
ENST00000578570.5:n.1610C>A
ENST00000579147.5:n.2515C>A
ENST00000580864.5:c.1176C>A	ENSP00000462495.1:p.Ser392=
ENST00000581882.5:c.1176C>A	ENSP00000463938.1:p.Ser392=
ENST00000584657.1:n.505C>A
ENST00000585242.5:c.*971C>A	ENSP00000463107.1:n.*971C>A
NM_001199163.1:c.1176C>A	NP_001186092.1:p.Ser392=
NM_002805.5:c.1200C>A	NP_002796.4:p.Ser400=
XM_006721980.1:c.1200C>A	XP_006722043.1:p.Ser400=
XR_934508.1:n.1289C>A
XM_024450840.1:c.1281C>A	XP_024306608.1:p.Ser427=
XM_024450841.1:c.1257C>A	XP_024306609.1:p.Ser419=
XR_934508.2:n.1276C>A
NM_002805.6:c.1200C>A MANE Select	NP_002796.4:p.Ser400=
NM_001199163.2:c.1176C>A	NP_001186092.1:p.Ser392=