Canonical Allele Identifier: CA2270102946

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831982T= , CM000679.2:g.63831982T=	GRCh38
NC_000017.10:g.61909342T= , CM000679.1:g.61909342T=	GRCh37
NC_000017.9:g.59263074T=	NCBI36
NG_053004.1:g.16010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*431T=	ENSP00000464347.2:n.*431T=
ENST00000703608.1:c.*751T=	ENSP00000515392.1:n.*751T=
ENST00000703609.1:c.*13T=	ENSP00000515393.1:n.*13T=
ENST00000703610.1:c.*511T=	ENSP00000515394.1:n.*511T=
ENST00000310144.11:c.*13T= MANE Select	ENSP00000310572.6:n.*13T=
ENST00000310144.10:c.*13T=	ENSP00000310572.6:n.*13T=
ENST00000375812.8:c.*13T=	ENSP00000364970.4:n.*13T=
ENST00000578570.5:n.1644T=
ENST00000579147.5:n.2549T=
ENST00000580864.5:c.*13T=	ENSP00000462495.1:n.*13T=
ENST00000581882.5:c.*13T=	ENSP00000463938.1:n.*13T=
ENST00000584657.1:n.539T=
ENST00000585242.5:c.*1005T=	ENSP00000463107.1:n.*1005T=
NM_001199163.1:c.*13T=	NP_001186092.1:n.*13T=
NM_002805.5:c.*13T=	NP_002796.4:n.*13T=
XM_006721980.1:c.*13T=	XP_006722043.1:n.*13T=
XR_934508.1:n.1323T=
XM_024450840.1:c.*13T=	XP_024306608.1:n.*13T=
XM_024450841.1:c.*13T=	XP_024306609.1:n.*13T=
XR_934508.2:n.1310T=
NM_002805.6:c.*13T= MANE Select	NP_002796.4:n.*13T=
NM_001199163.2:c.*13T=	NP_001186092.1:n.*13T=