Canonical Allele Identifier: CA400596602

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909300A>T (hg19) ; chr17:g.63831940A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831940A>T , CM000679.2:g.63831940A>T	GRCh38
NC_000017.10:g.61909300A>T , CM000679.1:g.61909300A>T	GRCh37
NC_000017.9:g.59263032A>T	NCBI36
NG_053004.1:g.16052T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*389A>T	ENSP00000464347.2:n.*389A>T
ENST00000703608.1:c.*709A>T	ENSP00000515392.1:n.*709A>T
ENST00000703609.1:c.1111A>T	ENSP00000515393.1:p.Asn371Tyr
ENST00000703610.1:c.*469A>T	ENSP00000515394.1:n.*469A>T
ENST00000310144.11:c.1192A>T MANE Select	ENSP00000310572.6:p.Asn398Tyr
ENST00000310144.10:c.1192A>T	ENSP00000310572.6:p.Asn398Tyr
ENST00000375812.8:c.1168A>T	ENSP00000364970.4:p.Asn390Tyr
ENST00000578570.5:n.1602A>T
ENST00000579147.5:n.2507A>T
ENST00000580864.5:c.1168A>T	ENSP00000462495.1:p.Asn390Tyr
ENST00000581882.5:c.1168A>T	ENSP00000463938.1:p.Asn390Tyr
ENST00000584657.1:n.497A>T
ENST00000585242.5:c.*963A>T	ENSP00000463107.1:n.*963A>T
NM_001199163.1:c.1168A>T	NP_001186092.1:p.Asn390Tyr
NM_002805.5:c.1192A>T	NP_002796.4:p.Asn398Tyr
XM_006721980.1:c.1192A>T	XP_006722043.1:p.Asn398Tyr
XR_934508.1:n.1281A>T
XM_024450840.1:c.1273A>T	XP_024306608.1:p.Asn425Tyr
XM_024450841.1:c.1249A>T	XP_024306609.1:p.Asn417Tyr
XR_934508.2:n.1268A>T
NM_002805.6:c.1192A>T MANE Select	NP_002796.4:p.Asn398Tyr
NM_001199163.2:c.1168A>T	NP_001186092.1:p.Asn390Tyr