Canonical Allele Identifier: CA773992895

Gene: PSMC5

Linked Data

• dbSNP Id: rs1189764815
• MyVariant Identifiers: chr17:g.61909348_61909349del (hg19) ; chr17:g.63831988_63831989del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831989_63831990del , CM000679.2:g.63831989_63831990del	GRCh38
NC_000017.10:g.61909349_61909350del , CM000679.1:g.61909349_61909350del	GRCh37
NC_000017.9:g.59263081_59263082del	NCBI36
NG_053004.1:g.16003_16004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*438_*439del	ENSP00000464347.2:n.*438_*439del
ENST00000703608.1:c.*758_*759del	ENSP00000515392.1:n.*758_*759del
ENST00000703609.1:c.*20_*21del	ENSP00000515393.1:n.*20_*21del
ENST00000703610.1:c.*518_*519del	ENSP00000515394.1:n.*518_*519del
ENST00000310144.11:c.*20_*21del MANE Select	ENSP00000310572.6:n.*20_*21del
ENST00000310144.10:c.*20_*21del	ENSP00000310572.6:n.*20_*21del
ENST00000375812.8:c.*20_*21del	ENSP00000364970.4:n.*20_*21del
ENST00000578570.5:n.1651_1652del
ENST00000579147.5:n.2556_2557del
ENST00000580864.5:c.*20_*21del	ENSP00000462495.1:n.*20_*21del
ENST00000584657.1:n.546_547del
NM_001199163.1:c.*20_*21del	NP_001186092.1:n.*20_*21del
NM_002805.5:c.*20_*21del	NP_002796.4:n.*20_*21del
XM_006721980.1:c.*20_*21del	XP_006722043.1:n.*20_*21del
XR_934508.1:n.1330_1331del
XM_024450840.1:c.*20_*21del	XP_024306608.1:n.*20_*21del
XM_024450841.1:c.*20_*21del	XP_024306609.1:n.*20_*21del
XR_934508.2:n.1317_1318del
NM_002805.6:c.*20_*21del MANE Select	NP_002796.4:n.*20_*21del
NM_001199163.2:c.*20_*21del	NP_001186092.1:n.*20_*21del