Canonical Allele Identifier: CA400596579

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909291A>C (hg19) ; chr17:g.63831931A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831931A>C , CM000679.2:g.63831931A>C	GRCh38
NC_000017.10:g.61909291A>C , CM000679.1:g.61909291A>C	GRCh37
NC_000017.9:g.59263023A>C	NCBI36
NG_053004.1:g.16061T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*380A>C	ENSP00000464347.2:n.*380A>C
ENST00000703608.1:c.*700A>C	ENSP00000515392.1:n.*700A>C
ENST00000703609.1:c.1102A>C	ENSP00000515393.1:p.Ser368Arg
ENST00000703610.1:c.*460A>C	ENSP00000515394.1:n.*460A>C
ENST00000310144.11:c.1183A>C MANE Select	ENSP00000310572.6:p.Ser395Arg
ENST00000310144.10:c.1183A>C	ENSP00000310572.6:p.Ser395Arg
ENST00000375812.8:c.1159A>C	ENSP00000364970.4:p.Ser387Arg
ENST00000578570.5:n.1593A>C
ENST00000579147.5:n.2498A>C
ENST00000580864.5:c.1159A>C	ENSP00000462495.1:p.Ser387Arg
ENST00000581882.5:c.1159A>C	ENSP00000463938.1:p.Ser387Arg
ENST00000584657.1:n.488A>C
ENST00000585242.5:c.*954A>C	ENSP00000463107.1:n.*954A>C
NM_001199163.1:c.1159A>C	NP_001186092.1:p.Ser387Arg
NM_002805.5:c.1183A>C	NP_002796.4:p.Ser395Arg
XM_006721980.1:c.1183A>C	XP_006722043.1:p.Ser395Arg
XR_934508.1:n.1272A>C
XM_024450840.1:c.1264A>C	XP_024306608.1:p.Ser422Arg
XM_024450841.1:c.1240A>C	XP_024306609.1:p.Ser414Arg
XR_934508.2:n.1259A>C
NM_002805.6:c.1183A>C MANE Select	NP_002796.4:p.Ser395Arg
NM_001199163.2:c.1159A>C	NP_001186092.1:p.Ser387Arg