Canonical Allele Identifier: CA501201559

Gene: PSMC5

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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