Canonical Allele Identifier: CA2270102902

Gene: PSMC5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831877T= , CM000679.2:g.63831877T=	GRCh38
NC_000017.10:g.61909237T= , CM000679.1:g.61909237T=	GRCh37
NC_000017.9:g.59262969T=	NCBI36
NG_053004.1:g.16115A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*365-39T=	ENSP00000464347.2:n.*365-39T=
ENST00000703608.1:c.*685-39T=	ENSP00000515392.1:n.*685-39T=
ENST00000703609.1:c.1087-39T=	ENSP00000515393.1:n.1087-39T=
ENST00000703610.1:c.*445-39T=	ENSP00000515394.1:n.*445-39T=
ENST00000310144.11:c.1168-39T= MANE Select	ENSP00000310572.6:n.1168-39T=
ENST00000310144.10:c.1168-39T=	ENSP00000310572.6:n.1168-39T=
ENST00000375812.8:c.1144-39T=	ENSP00000364970.4:n.1144-39T=
ENST00000578570.5:n.1578-39T=
ENST00000579147.5:n.2483-39T=
ENST00000580864.5:c.1144-39T=	ENSP00000462495.1:n.1144-39T=
ENST00000581882.5:c.1144-39T=	ENSP00000463938.1:n.1144-39T=
ENST00000584657.1:n.473-39T=
ENST00000585242.5:c.*939-39T=	ENSP00000463107.1:n.*939-39T=
NM_001199163.1:c.1144-39T=	NP_001186092.1:n.1144-39T=
NM_002805.5:c.1168-39T=	NP_002796.4:n.1168-39T=
XM_006721980.1:c.1168-39T=	XP_006722043.1:n.1168-39T=
XR_934508.1:n.1257-39T=
XM_024450840.1:c.1249-39T=	XP_024306608.1:n.1249-39T=
XM_024450841.1:c.1225-39T=	XP_024306609.1:n.1225-39T=
XR_934508.2:n.1244-39T=
NM_002805.6:c.1168-39T= MANE Select	NP_002796.4:n.1168-39T=
NM_001199163.2:c.1144-39T=	NP_001186092.1:n.1144-39T=