Canonical Allele Identifier: CA2270102929

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831919A= , CM000679.2:g.63831919A=	GRCh38
NC_000017.10:g.61909279A= , CM000679.1:g.61909279A=	GRCh37
NC_000017.9:g.59263011A=	NCBI36
NG_053004.1:g.16073T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*368A=	ENSP00000464347.2:n.*368A=
ENST00000703608.1:c.*688A=	ENSP00000515392.1:n.*688A=
ENST00000703609.1:c.1090A=	ENSP00000515393.1:p.Met364=
ENST00000703610.1:c.*448A=	ENSP00000515394.1:n.*448A=
ENST00000310144.11:c.1171A= MANE Select	ENSP00000310572.6:p.Met391=
ENST00000310144.10:c.1171A=	ENSP00000310572.6:p.Met391=
ENST00000375812.8:c.1147A=	ENSP00000364970.4:p.Met383=
ENST00000578570.5:n.1581A=
ENST00000579147.5:n.2486A=
ENST00000580864.5:c.1147A=	ENSP00000462495.1:p.Met383=
ENST00000581882.5:c.1147A=	ENSP00000463938.1:p.Met383=
ENST00000584657.1:n.476A=
ENST00000585242.5:c.*942A=	ENSP00000463107.1:n.*942A=
NM_001199163.1:c.1147A=	NP_001186092.1:p.Met383=
NM_002805.5:c.1171A=	NP_002796.4:p.Met391=
XM_006721980.1:c.1171A=	XP_006722043.1:p.Met391=
XR_934508.1:n.1260A=
XM_024450840.1:c.1252A=	XP_024306608.1:p.Met418=
XM_024450841.1:c.1228A=	XP_024306609.1:p.Met410=
XR_934508.2:n.1247A=
NM_002805.6:c.1171A= MANE Select	NP_002796.4:p.Met391=
NM_001199163.2:c.1147A=	NP_001186092.1:p.Met383=