Canonical Allele Identifier: CA400596582

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909292G>C (hg19) ; chr17:g.63831932G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831932G>C , CM000679.2:g.63831932G>C	GRCh38
NC_000017.10:g.61909292G>C , CM000679.1:g.61909292G>C	GRCh37
NC_000017.9:g.59263024G>C	NCBI36
NG_053004.1:g.16060C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*381G>C	ENSP00000464347.2:n.*381G>C
ENST00000703608.1:c.*701G>C	ENSP00000515392.1:n.*701G>C
ENST00000703609.1:c.1103G>C	ENSP00000515393.1:p.Ser368Thr
ENST00000703610.1:c.*461G>C	ENSP00000515394.1:n.*461G>C
ENST00000310144.11:c.1184G>C MANE Select	ENSP00000310572.6:p.Ser395Thr
ENST00000310144.10:c.1184G>C	ENSP00000310572.6:p.Ser395Thr
ENST00000375812.8:c.1160G>C	ENSP00000364970.4:p.Ser387Thr
ENST00000578570.5:n.1594G>C
ENST00000579147.5:n.2499G>C
ENST00000580864.5:c.1160G>C	ENSP00000462495.1:p.Ser387Thr
ENST00000581882.5:c.1160G>C	ENSP00000463938.1:p.Ser387Thr
ENST00000584657.1:n.489G>C
ENST00000585242.5:c.*955G>C	ENSP00000463107.1:n.*955G>C
NM_001199163.1:c.1160G>C	NP_001186092.1:p.Ser387Thr
NM_002805.5:c.1184G>C	NP_002796.4:p.Ser395Thr
XM_006721980.1:c.1184G>C	XP_006722043.1:p.Ser395Thr
XR_934508.1:n.1273G>C
XM_024450840.1:c.1265G>C	XP_024306608.1:p.Ser422Thr
XM_024450841.1:c.1241G>C	XP_024306609.1:p.Ser414Thr
XR_934508.2:n.1260G>C
NM_002805.6:c.1184G>C MANE Select	NP_002796.4:p.Ser395Thr
NM_001199163.2:c.1160G>C	NP_001186092.1:p.Ser387Thr