Canonical Allele Identifier: CA2270102968

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832017G= , CM000679.2:g.63832017G=	GRCh38
NC_000017.10:g.61909377G= , CM000679.1:g.61909377G=	GRCh37
NC_000017.9:g.59263109G=	NCBI36
NG_053004.1:g.15975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703608.1:c.*786G=	ENSP00000515392.1:n.*786G=
ENST00000703609.1:c.*48G=	ENSP00000515393.1:n.*48G=
ENST00000310144.11:c.*48G= MANE Select	ENSP00000310572.6:n.*48G=
ENST00000310144.10:c.*48G=	ENSP00000310572.6:n.*48G=
ENST00000375812.8:c.*48G=	ENSP00000364970.4:n.*48G=
ENST00000578570.5:n.1679G=
ENST00000579147.5:n.2584G=
ENST00000580864.5:c.*48G=	ENSP00000462495.1:n.*48G=
ENST00000584657.1:n.574G=
NM_001199163.1:c.*48G=	NP_001186092.1:n.*48G=
NM_002805.5:c.*48G=	NP_002796.4:n.*48G=
XM_006721980.1:c.*48G=	XP_006722043.1:n.*48G=
XR_934508.1:n.1358G=
XM_024450840.1:c.*48G=	XP_024306608.1:n.*48G=
XM_024450841.1:c.*48G=	XP_024306609.1:n.*48G=
XR_934508.2:n.1345G=
NM_002805.6:c.*48G= MANE Select	NP_002796.4:n.*48G=
NM_001199163.2:c.*48G=	NP_001186092.1:n.*48G=