Canonical Allele Identifier: CA501201563

Gene: PSMC5

Linked Data

• COSMIC: COSM349409
• MyVariant Identifiers: chr17:g.61909311C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831951C>T , CM000679.2:g.63831951C>T	GRCh38
NC_000017.10:g.61909311C>T , CM000679.1:g.61909311C>T	GRCh37
NC_000017.9:g.59263043C>T	NCBI36
NG_053004.1:g.16041G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*400C>T	ENSP00000464347.2:n.*400C>T
ENST00000703608.1:c.*720C>T	ENSP00000515392.1:n.*720C>T
ENST00000703609.1:c.1122C>T	ENSP00000515393.1:p.Ile374=
ENST00000703610.1:c.*480C>T	ENSP00000515394.1:n.*480C>T
ENST00000310144.11:c.1203C>T MANE Select	ENSP00000310572.6:p.Ile401=
ENST00000310144.10:c.1203C>T	ENSP00000310572.6:p.Ile401=
ENST00000375812.8:c.1179C>T	ENSP00000364970.4:p.Ile393=
ENST00000578570.5:n.1613C>T
ENST00000579147.5:n.2518C>T
ENST00000580864.5:c.1179C>T	ENSP00000462495.1:p.Ile393=
ENST00000581882.5:c.1179C>T	ENSP00000463938.1:p.Ile393=
ENST00000584657.1:n.508C>T
ENST00000585242.5:c.*974C>T	ENSP00000463107.1:n.*974C>T
NM_001199163.1:c.1179C>T	NP_001186092.1:p.Ile393=
NM_002805.5:c.1203C>T	NP_002796.4:p.Ile401=
XM_006721980.1:c.1203C>T	XP_006722043.1:p.Ile401=
XR_934508.1:n.1292C>T
XM_024450840.1:c.1284C>T	XP_024306608.1:p.Ile428=
XM_024450841.1:c.1260C>T	XP_024306609.1:p.Ile420=
XR_934508.2:n.1279C>T
NM_002805.6:c.1203C>T MANE Select	NP_002796.4:p.Ile401=
NM_001199163.2:c.1179C>T	NP_001186092.1:p.Ile393=