Canonical Allele Identifier: CA400596672

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909327T>C (hg19) ; chr17:g.63831967T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831967T>C , CM000679.2:g.63831967T>C	GRCh38
NC_000017.10:g.61909327T>C , CM000679.1:g.61909327T>C	GRCh37
NC_000017.9:g.59263059T>C	NCBI36
NG_053004.1:g.16025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*416T>C	ENSP00000464347.2:n.*416T>C
ENST00000703608.1:c.*736T>C	ENSP00000515392.1:n.*736T>C
ENST00000703609.1:c.1138T>C	ENSP00000515393.1:p.Ter380Arg
ENST00000703610.1:c.*496T>C	ENSP00000515394.1:n.*496T>C
ENST00000310144.11:c.1219T>C MANE Select	ENSP00000310572.6:p.Ter407Arg
ENST00000310144.10:c.1219T>C	ENSP00000310572.6:p.Ter407Arg
ENST00000375812.8:c.1195T>C	ENSP00000364970.4:p.Ter399Arg
ENST00000578570.5:n.1629T>C
ENST00000579147.5:n.2534T>C
ENST00000580864.5:c.1195T>C	ENSP00000462495.1:p.Ter399Arg
ENST00000581882.5:c.1195T>C	ENSP00000463938.1:p.Ter399Arg
ENST00000584657.1:n.524T>C
ENST00000585242.5:c.*990T>C	ENSP00000463107.1:n.*990T>C
NM_001199163.1:c.1195T>C	NP_001186092.1:p.Ter399Arg
NM_002805.5:c.1219T>C	NP_002796.4:p.Ter407Arg
XM_006721980.1:c.1219T>C	XP_006722043.1:p.Ter407Arg
XR_934508.1:n.1308T>C
XM_024450840.1:c.1300T>C	XP_024306608.1:p.Ter434Arg
XM_024450841.1:c.1276T>C	XP_024306609.1:p.Ter426Arg
XR_934508.2:n.1295T>C
NM_002805.6:c.1219T>C MANE Select	NP_002796.4:p.Ter407Arg
NM_001199163.2:c.1195T>C	NP_001186092.1:p.Ter399Arg