Canonical Allele Identifier: CA2270102940

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831973G= , CM000679.2:g.63831973G=	GRCh38
NC_000017.10:g.61909333G= , CM000679.1:g.61909333G=	GRCh37
NC_000017.9:g.59263065G=	NCBI36
NG_053004.1:g.16019C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*422G=	ENSP00000464347.2:n.*422G=
ENST00000703608.1:c.*742G=	ENSP00000515392.1:n.*742G=
ENST00000703609.1:c.*4G=	ENSP00000515393.1:n.*4G=
ENST00000703610.1:c.*502G=	ENSP00000515394.1:n.*502G=
ENST00000310144.11:c.*4G= MANE Select	ENSP00000310572.6:n.*4G=
ENST00000310144.10:c.*4G=	ENSP00000310572.6:n.*4G=
ENST00000375812.8:c.*4G=	ENSP00000364970.4:n.*4G=
ENST00000578570.5:n.1635G=
ENST00000579147.5:n.2540G=
ENST00000580864.5:c.*4G=	ENSP00000462495.1:n.*4G=
ENST00000581882.5:c.*4G=	ENSP00000463938.1:n.*4G=
ENST00000584657.1:n.530G=
ENST00000585242.5:c.*996G=	ENSP00000463107.1:n.*996G=
NM_001199163.1:c.*4G=	NP_001186092.1:n.*4G=
NM_002805.5:c.*4G=	NP_002796.4:n.*4G=
XM_006721980.1:c.*4G=	XP_006722043.1:n.*4G=
XR_934508.1:n.1314G=
XM_024450840.1:c.*4G=	XP_024306608.1:n.*4G=
XM_024450841.1:c.*4G=	XP_024306609.1:n.*4G=
XR_934508.2:n.1301G=
NM_002805.6:c.*4G= MANE Select	NP_002796.4:n.*4G=
NM_001199163.2:c.*4G=	NP_001186092.1:n.*4G=