Canonical Allele Identifier: CA400596656

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909321T>G (hg19) ; chr17:g.63831961T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831961T>G , CM000679.2:g.63831961T>G	GRCh38
NC_000017.10:g.61909321T>G , CM000679.1:g.61909321T>G	GRCh37
NC_000017.9:g.59263053T>G	NCBI36
NG_053004.1:g.16031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*410T>G	ENSP00000464347.2:n.*410T>G
ENST00000703608.1:c.*730T>G	ENSP00000515392.1:n.*730T>G
ENST00000703609.1:c.1132T>G	ENSP00000515393.1:p.Trp378Gly
ENST00000703610.1:c.*490T>G	ENSP00000515394.1:n.*490T>G
ENST00000310144.11:c.1213T>G MANE Select	ENSP00000310572.6:p.Trp405Gly
ENST00000310144.10:c.1213T>G	ENSP00000310572.6:p.Trp405Gly
ENST00000375812.8:c.1189T>G	ENSP00000364970.4:p.Trp397Gly
ENST00000578570.5:n.1623T>G
ENST00000579147.5:n.2528T>G
ENST00000580864.5:c.1189T>G	ENSP00000462495.1:p.Trp397Gly
ENST00000581882.5:c.1189T>G	ENSP00000463938.1:p.Trp397Gly
ENST00000584657.1:n.518T>G
ENST00000585242.5:c.*984T>G	ENSP00000463107.1:n.*984T>G
NM_001199163.1:c.1189T>G	NP_001186092.1:p.Trp397Gly
NM_002805.5:c.1213T>G	NP_002796.4:p.Trp405Gly
XM_006721980.1:c.1213T>G	XP_006722043.1:p.Trp405Gly
XR_934508.1:n.1302T>G
XM_024450840.1:c.1294T>G	XP_024306608.1:p.Trp432Gly
XM_024450841.1:c.1270T>G	XP_024306609.1:p.Trp424Gly
XR_934508.2:n.1289T>G
NM_002805.6:c.1213T>G MANE Select	NP_002796.4:p.Trp405Gly
NM_001199163.2:c.1189T>G	NP_001186092.1:p.Trp397Gly