Canonical Allele Identifier: CA400596614
Gene: PSMC5 HGNC NCBI

Linked Data

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