Canonical Allele Identifier: CA2270102931

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831923A= , CM000679.2:g.63831923A=	GRCh38
NC_000017.10:g.61909283A= , CM000679.1:g.61909283A=	GRCh37
NC_000017.9:g.59263015A=	NCBI36
NG_053004.1:g.16069T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*372A=	ENSP00000464347.2:n.*372A=
ENST00000703608.1:c.*692A=	ENSP00000515392.1:n.*692A=
ENST00000703609.1:c.1094A=	ENSP00000515393.1:p.Gln365=
ENST00000703610.1:c.*452A=	ENSP00000515394.1:n.*452A=
ENST00000310144.11:c.1175A= MANE Select	ENSP00000310572.6:p.Gln392=
ENST00000310144.10:c.1175A=	ENSP00000310572.6:p.Gln392=
ENST00000375812.8:c.1151A=	ENSP00000364970.4:p.Gln384=
ENST00000578570.5:n.1585A=
ENST00000579147.5:n.2490A=
ENST00000580864.5:c.1151A=	ENSP00000462495.1:p.Gln384=
ENST00000581882.5:c.1151A=	ENSP00000463938.1:p.Gln384=
ENST00000584657.1:n.480A=
ENST00000585242.5:c.*946A=	ENSP00000463107.1:n.*946A=
NM_001199163.1:c.1151A=	NP_001186092.1:p.Gln384=
NM_002805.5:c.1175A=	NP_002796.4:p.Gln392=
XM_006721980.1:c.1175A=	XP_006722043.1:p.Gln392=
XR_934508.1:n.1264A=
XM_024450840.1:c.1256A=	XP_024306608.1:p.Gln419=
XM_024450841.1:c.1232A=	XP_024306609.1:p.Gln411=
XR_934508.2:n.1251A=
NM_002805.6:c.1175A= MANE Select	NP_002796.4:p.Gln392=
NM_001199163.2:c.1151A=	NP_001186092.1:p.Gln384=