Canonical Allele Identifier: CA501201555

Gene: PSMC5

Linked Data

• MyVariant Identifiers: chr17:g.61909293T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63831933T>C , CM000679.2:g.63831933T>C	GRCh38
NC_000017.10:g.61909293T>C , CM000679.1:g.61909293T>C	GRCh37
NC_000017.9:g.59263025T>C	NCBI36
NG_053004.1:g.16059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584880.6:c.*382T>C	ENSP00000464347.2:n.*382T>C
ENST00000703608.1:c.*702T>C	ENSP00000515392.1:n.*702T>C
ENST00000703609.1:c.1104T>C	ENSP00000515393.1:p.Ser368=
ENST00000703610.1:c.*462T>C	ENSP00000515394.1:n.*462T>C
ENST00000310144.11:c.1185T>C MANE Select	ENSP00000310572.6:p.Ser395=
ENST00000310144.10:c.1185T>C	ENSP00000310572.6:p.Ser395=
ENST00000375812.8:c.1161T>C	ENSP00000364970.4:p.Ser387=
ENST00000578570.5:n.1595T>C
ENST00000579147.5:n.2500T>C
ENST00000580864.5:c.1161T>C	ENSP00000462495.1:p.Ser387=
ENST00000581882.5:c.1161T>C	ENSP00000463938.1:p.Ser387=
ENST00000584657.1:n.490T>C
ENST00000585242.5:c.*956T>C	ENSP00000463107.1:n.*956T>C
NM_001199163.1:c.1161T>C	NP_001186092.1:p.Ser387=
NM_002805.5:c.1185T>C	NP_002796.4:p.Ser395=
XM_006721980.1:c.1185T>C	XP_006722043.1:p.Ser395=
XR_934508.1:n.1274T>C
XM_024450840.1:c.1266T>C	XP_024306608.1:p.Ser422=
XM_024450841.1:c.1242T>C	XP_024306609.1:p.Ser414=
XR_934508.2:n.1261T>C
NM_002805.6:c.1185T>C MANE Select	NP_002796.4:p.Ser395=
NM_001199163.2:c.1161T>C	NP_001186092.1:p.Ser387=