Canonical Allele Identifier: CA2639297904

Gene: PSMC5

Linked Data

• gnomAD v4: 17-63832016-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832016A>G , CM000679.2:g.63832016A>G	GRCh38
NC_000017.10:g.61909376A>G , CM000679.1:g.61909376A>G	GRCh37
NC_000017.9:g.59263108A>G	NCBI36
NG_053004.1:g.15976T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703608.1:c.*785A>G	ENSP00000515392.1:n.*785A>G
ENST00000703609.1:c.*47A>G	ENSP00000515393.1:n.*47A>G
ENST00000310144.11:c.*47A>G MANE Select	ENSP00000310572.6:n.*47A>G
ENST00000310144.10:c.*47A>G	ENSP00000310572.6:n.*47A>G
ENST00000375812.8:c.*47A>G	ENSP00000364970.4:n.*47A>G
ENST00000578570.5:n.1678A>G
ENST00000579147.5:n.2583A>G
ENST00000580864.5:c.*47A>G	ENSP00000462495.1:n.*47A>G
ENST00000584657.1:n.573A>G
NM_001199163.1:c.*47A>G	NP_001186092.1:n.*47A>G
NM_002805.5:c.*47A>G	NP_002796.4:n.*47A>G
XM_006721980.1:c.*47A>G	XP_006722043.1:n.*47A>G
XR_934508.1:n.1357A>G
XM_024450840.1:c.*47A>G	XP_024306608.1:n.*47A>G
XM_024450841.1:c.*47A>G	XP_024306609.1:n.*47A>G
XR_934508.2:n.1344A>G
NM_002805.6:c.*47A>G MANE Select	NP_002796.4:n.*47A>G
NM_001199163.2:c.*47A>G	NP_001186092.1:n.*47A>G