Canonical Allele Identifier: CA400596665

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909324A>C (hg19) ; chr17:g.63831964A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831964A>C , CM000679.2:g.63831964A>C	GRCh38
NC_000017.10:g.61909324A>C , CM000679.1:g.61909324A>C	GRCh37
NC_000017.9:g.59263056A>C	NCBI36
NG_053004.1:g.16028T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*413A>C	ENSP00000464347.2:n.*413A>C
ENST00000703608.1:c.*733A>C	ENSP00000515392.1:n.*733A>C
ENST00000703609.1:c.1135A>C	ENSP00000515393.1:p.Lys379Gln
ENST00000703610.1:c.*493A>C	ENSP00000515394.1:n.*493A>C
ENST00000310144.11:c.1216A>C MANE Select	ENSP00000310572.6:p.Lys406Gln
ENST00000310144.10:c.1216A>C	ENSP00000310572.6:p.Lys406Gln
ENST00000375812.8:c.1192A>C	ENSP00000364970.4:p.Lys398Gln
ENST00000578570.5:n.1626A>C
ENST00000579147.5:n.2531A>C
ENST00000580864.5:c.1192A>C	ENSP00000462495.1:p.Lys398Gln
ENST00000581882.5:c.1192A>C	ENSP00000463938.1:p.Lys398Gln
ENST00000584657.1:n.521A>C
ENST00000585242.5:c.*987A>C	ENSP00000463107.1:n.*987A>C
NM_001199163.1:c.1192A>C	NP_001186092.1:p.Lys398Gln
NM_002805.5:c.1216A>C	NP_002796.4:p.Lys406Gln
XM_006721980.1:c.1216A>C	XP_006722043.1:p.Lys406Gln
XR_934508.1:n.1305A>C
XM_024450840.1:c.1297A>C	XP_024306608.1:p.Lys433Gln
XM_024450841.1:c.1273A>C	XP_024306609.1:p.Lys425Gln
XR_934508.2:n.1292A>C
NM_002805.6:c.1216A>C MANE Select	NP_002796.4:p.Lys406Gln
NM_001199163.2:c.1192A>C	NP_001186092.1:p.Lys398Gln