Canonical Allele Identifier: CA2270102954

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831988T= , CM000679.2:g.63831988T=	GRCh38
NC_000017.10:g.61909348T= , CM000679.1:g.61909348T=	GRCh37
NC_000017.9:g.59263080T=	NCBI36
NG_053004.1:g.16004A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*437T=	ENSP00000464347.2:n.*437T=
ENST00000703608.1:c.*757T=	ENSP00000515392.1:n.*757T=
ENST00000703609.1:c.*19T=	ENSP00000515393.1:n.*19T=
ENST00000703610.1:c.*517T=	ENSP00000515394.1:n.*517T=
ENST00000310144.11:c.*19T= MANE Select	ENSP00000310572.6:n.*19T=
ENST00000310144.10:c.*19T=	ENSP00000310572.6:n.*19T=
ENST00000375812.8:c.*19T=	ENSP00000364970.4:n.*19T=
ENST00000578570.5:n.1650T=
ENST00000579147.5:n.2555T=
ENST00000580864.5:c.*19T=	ENSP00000462495.1:n.*19T=
ENST00000584657.1:n.545T=
NM_001199163.1:c.*19T=	NP_001186092.1:n.*19T=
NM_002805.5:c.*19T=	NP_002796.4:n.*19T=
XM_006721980.1:c.*19T=	XP_006722043.1:n.*19T=
XR_934508.1:n.1329T=
XM_024450840.1:c.*19T=	XP_024306608.1:n.*19T=
XM_024450841.1:c.*19T=	XP_024306609.1:n.*19T=
XR_934508.2:n.1316T=
NM_002805.6:c.*19T= MANE Select	NP_002796.4:n.*19T=
NM_001199163.2:c.*19T=	NP_001186092.1:n.*19T=