Canonical Allele Identifier: CA400596614

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909304T>G (hg19) ; chr17:g.63831944T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831944T>G , CM000679.2:g.63831944T>G	GRCh38
NC_000017.10:g.61909304T>G , CM000679.1:g.61909304T>G	GRCh37
NC_000017.9:g.59263036T>G	NCBI36
NG_053004.1:g.16048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*393T>G	ENSP00000464347.2:n.*393T>G
ENST00000703608.1:c.*713T>G	ENSP00000515392.1:n.*713T>G
ENST00000703609.1:c.1115T>G	ENSP00000515393.1:p.Met372Arg
ENST00000703610.1:c.*473T>G	ENSP00000515394.1:n.*473T>G
ENST00000310144.11:c.1196T>G MANE Select	ENSP00000310572.6:p.Met399Arg
ENST00000310144.10:c.1196T>G	ENSP00000310572.6:p.Met399Arg
ENST00000375812.8:c.1172T>G	ENSP00000364970.4:p.Met391Arg
ENST00000578570.5:n.1606T>G
ENST00000579147.5:n.2511T>G
ENST00000580864.5:c.1172T>G	ENSP00000462495.1:p.Met391Arg
ENST00000581882.5:c.1172T>G	ENSP00000463938.1:p.Met391Arg
ENST00000584657.1:n.501T>G
ENST00000585242.5:c.*967T>G	ENSP00000463107.1:n.*967T>G
NM_001199163.1:c.1172T>G	NP_001186092.1:p.Met391Arg
NM_002805.5:c.1196T>G	NP_002796.4:p.Met399Arg
XM_006721980.1:c.1196T>G	XP_006722043.1:p.Met399Arg
XR_934508.1:n.1285T>G
XM_024450840.1:c.1277T>G	XP_024306608.1:p.Met426Arg
XM_024450841.1:c.1253T>G	XP_024306609.1:p.Met418Arg
XR_934508.2:n.1272T>G
NM_002805.6:c.1196T>G MANE Select	NP_002796.4:p.Met399Arg
NM_001199163.2:c.1172T>G	NP_001186092.1:p.Met391Arg