Canonical Allele Identifier: CA2270102935

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831939A= , CM000679.2:g.63831939A=	GRCh38
NC_000017.10:g.61909299A= , CM000679.1:g.61909299A=	GRCh37
NC_000017.9:g.59263031A=	NCBI36
NG_053004.1:g.16053T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*388A=	ENSP00000464347.2:n.*388A=
ENST00000703608.1:c.*708A=	ENSP00000515392.1:n.*708A=
ENST00000703609.1:c.1110A=	ENSP00000515393.1:p.Lys370=
ENST00000703610.1:c.*468A=	ENSP00000515394.1:n.*468A=
ENST00000310144.11:c.1191A= MANE Select	ENSP00000310572.6:p.Lys397=
ENST00000310144.10:c.1191A=	ENSP00000310572.6:p.Lys397=
ENST00000375812.8:c.1167A=	ENSP00000364970.4:p.Lys389=
ENST00000578570.5:n.1601A=
ENST00000579147.5:n.2506A=
ENST00000580864.5:c.1167A=	ENSP00000462495.1:p.Lys389=
ENST00000581882.5:c.1167A=	ENSP00000463938.1:p.Lys389=
ENST00000584657.1:n.496A=
ENST00000585242.5:c.*962A=	ENSP00000463107.1:n.*962A=
NM_001199163.1:c.1167A=	NP_001186092.1:p.Lys389=
NM_002805.5:c.1191A=	NP_002796.4:p.Lys397=
XM_006721980.1:c.1191A=	XP_006722043.1:p.Lys397=
XR_934508.1:n.1280A=
XM_024450840.1:c.1272A=	XP_024306608.1:p.Lys424=
XM_024450841.1:c.1248A=	XP_024306609.1:p.Lys416=
XR_934508.2:n.1267A=
NM_002805.6:c.1191A= MANE Select	NP_002796.4:p.Lys397=
NM_001199163.2:c.1167A=	NP_001186092.1:p.Lys389=