Canonical Allele Identifier: CA2270102928

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831916G= , CM000679.2:g.63831916G=	GRCh38
NC_000017.10:g.61909276G= , CM000679.1:g.61909276G=	GRCh37
NC_000017.9:g.59263008G=	NCBI36
NG_053004.1:g.16076C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*365G=	ENSP00000464347.2:n.*365G=
ENST00000703608.1:c.*685G=	ENSP00000515392.1:n.*685G=
ENST00000703609.1:c.1087G=	ENSP00000515393.1:p.Val363=
ENST00000703610.1:c.*445G=	ENSP00000515394.1:n.*445G=
ENST00000310144.11:c.1168G= MANE Select	ENSP00000310572.6:p.Val390=
ENST00000310144.10:c.1168G=	ENSP00000310572.6:p.Val390=
ENST00000375812.8:c.1144G=	ENSP00000364970.4:p.Val382=
ENST00000578570.5:n.1578G=
ENST00000579147.5:n.2483G=
ENST00000580864.5:c.1144G=	ENSP00000462495.1:p.Val382=
ENST00000581882.5:c.1144G=	ENSP00000463938.1:p.Val382=
ENST00000584657.1:n.473G=
ENST00000585242.5:c.*939G=	ENSP00000463107.1:n.*939G=
NM_001199163.1:c.1144G=	NP_001186092.1:p.Val382=
NM_002805.5:c.1168G=	NP_002796.4:p.Val390=
XM_006721980.1:c.1168G=	XP_006722043.1:p.Val390=
XR_934508.1:n.1257G=
XM_024450840.1:c.1249G=	XP_024306608.1:p.Val417=
XM_024450841.1:c.1225G=	XP_024306609.1:p.Val409=
XR_934508.2:n.1244G=
NM_002805.6:c.1168G= MANE Select	NP_002796.4:p.Val390=
NM_001199163.2:c.1144G=	NP_001186092.1:p.Val382=