Canonical Allele Identifier: CA2270102950

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831986T= , CM000679.2:g.63831986T=	GRCh38
NC_000017.10:g.61909346T= , CM000679.1:g.61909346T=	GRCh37
NC_000017.9:g.59263078T=	NCBI36
NG_053004.1:g.16006A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*435T=	ENSP00000464347.2:n.*435T=
ENST00000703608.1:c.*755T=	ENSP00000515392.1:n.*755T=
ENST00000703609.1:c.*17T=	ENSP00000515393.1:n.*17T=
ENST00000703610.1:c.*515T=	ENSP00000515394.1:n.*515T=
ENST00000310144.11:c.*17T= MANE Select	ENSP00000310572.6:n.*17T=
ENST00000310144.10:c.*17T=	ENSP00000310572.6:n.*17T=
ENST00000375812.8:c.*17T=	ENSP00000364970.4:n.*17T=
ENST00000578570.5:n.1648T=
ENST00000579147.5:n.2553T=
ENST00000580864.5:c.*17T=	ENSP00000462495.1:n.*17T=
ENST00000581882.5:c.*17T=	ENSP00000463938.1:n.*17T=
ENST00000584657.1:n.543T=
NM_001199163.1:c.*17T=	NP_001186092.1:n.*17T=
NM_002805.5:c.*17T=	NP_002796.4:n.*17T=
XM_006721980.1:c.*17T=	XP_006722043.1:n.*17T=
XR_934508.1:n.1327T=
XM_024450840.1:c.*17T=	XP_024306608.1:n.*17T=
XM_024450841.1:c.*17T=	XP_024306609.1:n.*17T=
XR_934508.2:n.1314T=
NM_002805.6:c.*17T= MANE Select	NP_002796.4:n.*17T=
NM_001199163.2:c.*17T=	NP_001186092.1:n.*17T=