Canonical Allele Identifier: CA2270102932

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831924G= , CM000679.2:g.63831924G=	GRCh38
NC_000017.10:g.61909284G= , CM000679.1:g.61909284G=	GRCh37
NC_000017.9:g.59263016G=	NCBI36
NG_053004.1:g.16068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*373G=	ENSP00000464347.2:n.*373G=
ENST00000703608.1:c.*693G=	ENSP00000515392.1:n.*693G=
ENST00000703609.1:c.1095G=	ENSP00000515393.1:p.Gln365=
ENST00000703610.1:c.*453G=	ENSP00000515394.1:n.*453G=
ENST00000310144.11:c.1176G= MANE Select	ENSP00000310572.6:p.Gln392=
ENST00000310144.10:c.1176G=	ENSP00000310572.6:p.Gln392=
ENST00000375812.8:c.1152G=	ENSP00000364970.4:p.Gln384=
ENST00000578570.5:n.1586G=
ENST00000579147.5:n.2491G=
ENST00000580864.5:c.1152G=	ENSP00000462495.1:p.Gln384=
ENST00000581882.5:c.1152G=	ENSP00000463938.1:p.Gln384=
ENST00000584657.1:n.481G=
ENST00000585242.5:c.*947G=	ENSP00000463107.1:n.*947G=
NM_001199163.1:c.1152G=	NP_001186092.1:p.Gln384=
NM_002805.5:c.1176G=	NP_002796.4:p.Gln392=
XM_006721980.1:c.1176G=	XP_006722043.1:p.Gln392=
XR_934508.1:n.1265G=
XM_024450840.1:c.1257G=	XP_024306608.1:p.Gln419=
XM_024450841.1:c.1233G=	XP_024306609.1:p.Gln411=
XR_934508.2:n.1252G=
NM_002805.6:c.1176G= MANE Select	NP_002796.4:p.Gln392=
NM_001199163.2:c.1152G=	NP_001186092.1:p.Gln384=