Canonical Allele Identifier: CA2639297892

Gene: PSMC5

Linked Data

• gnomAD v4: 17-63831977-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831977G>T , CM000679.2:g.63831977G>T	GRCh38
NC_000017.10:g.61909337G>T , CM000679.1:g.61909337G>T	GRCh37
NC_000017.9:g.59263069G>T	NCBI36
NG_053004.1:g.16015C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*426G>T	ENSP00000464347.2:n.*426G>T
ENST00000703608.1:c.*746G>T	ENSP00000515392.1:n.*746G>T
ENST00000703609.1:c.*8G>T	ENSP00000515393.1:n.*8G>T
ENST00000703610.1:c.*506G>T	ENSP00000515394.1:n.*506G>T
ENST00000310144.11:c.*8G>T MANE Select	ENSP00000310572.6:n.*8G>T
ENST00000310144.10:c.*8G>T	ENSP00000310572.6:n.*8G>T
ENST00000375812.8:c.*8G>T	ENSP00000364970.4:n.*8G>T
ENST00000578570.5:n.1639G>T
ENST00000579147.5:n.2544G>T
ENST00000580864.5:c.*8G>T	ENSP00000462495.1:n.*8G>T
ENST00000581882.5:c.*8G>T	ENSP00000463938.1:n.*8G>T
ENST00000584657.1:n.534G>T
ENST00000585242.5:c.*1000G>T	ENSP00000463107.1:n.*1000G>T
NM_001199163.1:c.*8G>T	NP_001186092.1:n.*8G>T
NM_002805.5:c.*8G>T	NP_002796.4:n.*8G>T
XM_006721980.1:c.*8G>T	XP_006722043.1:n.*8G>T
XR_934508.1:n.1318G>T
XM_024450840.1:c.*8G>T	XP_024306608.1:n.*8G>T
XM_024450841.1:c.*8G>T	XP_024306609.1:n.*8G>T
XR_934508.2:n.1305G>T
NM_002805.6:c.*8G>T MANE Select	NP_002796.4:n.*8G>T
NM_001199163.2:c.*8G>T	NP_001186092.1:n.*8G>T