Canonical Allele Identifier: CA501201552

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909278C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831918C>T , CM000679.2:g.63831918C>T	GRCh38
NC_000017.10:g.61909278C>T , CM000679.1:g.61909278C>T	GRCh37
NC_000017.9:g.59263010C>T	NCBI36
NG_053004.1:g.16074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*367C>T	ENSP00000464347.2:n.*367C>T
ENST00000703608.1:c.*687C>T	ENSP00000515392.1:n.*687C>T
ENST00000703609.1:c.1089C>T	ENSP00000515393.1:p.Val363=
ENST00000703610.1:c.*447C>T	ENSP00000515394.1:n.*447C>T
ENST00000310144.11:c.1170C>T MANE Select	ENSP00000310572.6:p.Val390=
ENST00000310144.10:c.1170C>T	ENSP00000310572.6:p.Val390=
ENST00000375812.8:c.1146C>T	ENSP00000364970.4:p.Val382=
ENST00000578570.5:n.1580C>T
ENST00000579147.5:n.2485C>T
ENST00000580864.5:c.1146C>T	ENSP00000462495.1:p.Val382=
ENST00000581882.5:c.1146C>T	ENSP00000463938.1:p.Val382=
ENST00000584657.1:n.475C>T
ENST00000585242.5:c.*941C>T	ENSP00000463107.1:n.*941C>T
NM_001199163.1:c.1146C>T	NP_001186092.1:p.Val382=
NM_002805.5:c.1170C>T	NP_002796.4:p.Val390=
XM_006721980.1:c.1170C>T	XP_006722043.1:p.Val390=
XR_934508.1:n.1259C>T
XM_024450840.1:c.1251C>T	XP_024306608.1:p.Val417=
XM_024450841.1:c.1227C>T	XP_024306609.1:p.Val409=
XR_934508.2:n.1246C>T
NM_002805.6:c.1170C>T MANE Select	NP_002796.4:p.Val390=
NM_001199163.2:c.1146C>T	NP_001186092.1:p.Val382=