Canonical Allele Identifier: CA2270102957

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831990T= , CM000679.2:g.63831990T=	GRCh38
NC_000017.10:g.61909350T= , CM000679.1:g.61909350T=	GRCh37
NC_000017.9:g.59263082T=	NCBI36
NG_053004.1:g.16002A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*439T=	ENSP00000464347.2:n.*439T=
ENST00000703608.1:c.*759T=	ENSP00000515392.1:n.*759T=
ENST00000703609.1:c.*21T=	ENSP00000515393.1:n.*21T=
ENST00000703610.1:c.*519T=	ENSP00000515394.1:n.*519T=
ENST00000310144.11:c.*21T= MANE Select	ENSP00000310572.6:n.*21T=
ENST00000310144.10:c.*21T=	ENSP00000310572.6:n.*21T=
ENST00000375812.8:c.*21T=	ENSP00000364970.4:n.*21T=
ENST00000578570.5:n.1652T=
ENST00000579147.5:n.2557T=
ENST00000580864.5:c.*21T=	ENSP00000462495.1:n.*21T=
ENST00000584657.1:n.547T=
NM_001199163.1:c.*21T=	NP_001186092.1:n.*21T=
NM_002805.5:c.*21T=	NP_002796.4:n.*21T=
XM_006721980.1:c.*21T=	XP_006722043.1:n.*21T=
XR_934508.1:n.1331T=
XM_024450840.1:c.*21T=	XP_024306608.1:n.*21T=
XM_024450841.1:c.*21T=	XP_024306609.1:n.*21T=
XR_934508.2:n.1318T=
NM_002805.6:c.*21T= MANE Select	NP_002796.4:n.*21T=
NM_001199163.2:c.*21T=	NP_001186092.1:n.*21T=