Canonical Allele Identifier: CA2270102964

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832010G= , CM000679.2:g.63832010G=	GRCh38
NC_000017.10:g.61909370G= , CM000679.1:g.61909370G=	GRCh37
NC_000017.9:g.59263102G=	NCBI36
NG_053004.1:g.15982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703608.1:c.*779G=	ENSP00000515392.1:n.*779G=
ENST00000703609.1:c.*41G=	ENSP00000515393.1:n.*41G=
ENST00000310144.11:c.*41G= MANE Select	ENSP00000310572.6:n.*41G=
ENST00000310144.10:c.*41G=	ENSP00000310572.6:n.*41G=
ENST00000375812.8:c.*41G=	ENSP00000364970.4:n.*41G=
ENST00000578570.5:n.1672G=
ENST00000579147.5:n.2577G=
ENST00000580864.5:c.*41G=	ENSP00000462495.1:n.*41G=
ENST00000584657.1:n.567G=
NM_001199163.1:c.*41G=	NP_001186092.1:n.*41G=
NM_002805.5:c.*41G=	NP_002796.4:n.*41G=
XM_006721980.1:c.*41G=	XP_006722043.1:n.*41G=
XR_934508.1:n.1351G=
XM_024450840.1:c.*41G=	XP_024306608.1:n.*41G=
XM_024450841.1:c.*41G=	XP_024306609.1:n.*41G=
XR_934508.2:n.1338G=
NM_002805.6:c.*41G= MANE Select	NP_002796.4:n.*41G=
NM_001199163.2:c.*41G=	NP_001186092.1:n.*41G=