Canonical Allele Identifier: CA2270102938

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831944T= , CM000679.2:g.63831944T=	GRCh38
NC_000017.10:g.61909304T= , CM000679.1:g.61909304T=	GRCh37
NC_000017.9:g.59263036T=	NCBI36
NG_053004.1:g.16048A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*393T=	ENSP00000464347.2:n.*393T=
ENST00000703608.1:c.*713T=	ENSP00000515392.1:n.*713T=
ENST00000703609.1:c.1115T=	ENSP00000515393.1:p.Met372=
ENST00000703610.1:c.*473T=	ENSP00000515394.1:n.*473T=
ENST00000310144.11:c.1196T= MANE Select	ENSP00000310572.6:p.Met399=
ENST00000310144.10:c.1196T=	ENSP00000310572.6:p.Met399=
ENST00000375812.8:c.1172T=	ENSP00000364970.4:p.Met391=
ENST00000578570.5:n.1606T=
ENST00000579147.5:n.2511T=
ENST00000580864.5:c.1172T=	ENSP00000462495.1:p.Met391=
ENST00000581882.5:c.1172T=	ENSP00000463938.1:p.Met391=
ENST00000584657.1:n.501T=
ENST00000585242.5:c.*967T=	ENSP00000463107.1:n.*967T=
NM_001199163.1:c.1172T=	NP_001186092.1:p.Met391=
NM_002805.5:c.1196T=	NP_002796.4:p.Met399=
XM_006721980.1:c.1196T=	XP_006722043.1:p.Met399=
XR_934508.1:n.1285T=
XM_024450840.1:c.1277T=	XP_024306608.1:p.Met426=
XM_024450841.1:c.1253T=	XP_024306609.1:p.Met418=
XR_934508.2:n.1272T=
NM_002805.6:c.1196T= MANE Select	NP_002796.4:p.Met399=
NM_001199163.2:c.1172T=	NP_001186092.1:p.Met391=