Canonical Allele Identifier: CA917718147

Gene: PSMB8

Linked Data

• dbSNP Id: rs1554239569

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842773_32842774delinsTT , CM000668.2:g.32842773_32842774delinsTT	GRCh38
NC_000006.11:g.32810550_32810551delinsTT , CM000668.1:g.32810550_32810551delinsTT	GRCh37
NC_000006.10:g.32918528_32918529delinsTT	NCBI36
NG_009793.3:g.997_998delinsAA
NG_028165.1:g.7162_7163delinsAA
NG_009793.4:g.997_998delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.484_485delinsAA
ENST00000697612.1:n.1162_1163delinsAA
ENST00000374881.3:c.293_294delinsAA	ENSP00000364015.2:p.Arg98Gln
ENST00000374882.8:c.305_306delinsAA MANE Select	ENSP00000364016.4:p.Arg102Gln
ENST00000650411.1:n.1626_1627delinsAA
ENST00000650793.1:n.484_485delinsAA
ENST00000374881.2:c.293_294delinsAA	ENSP00000364015.2:p.Arg98Gln
ENST00000374882.7:c.305_306delinsAA	ENSP00000364016.3:p.Arg102Gln
ENST00000395339.7:c.296-63_296-62delinsAA	ENSP00000378748.3:n.296-63_296-62delinsAA
ENST00000484003.1:n.689_690delinsAA
NM_004159.4:c.293_294delinsAA	NP_004150.1:p.Arg98Gln
NM_148919.3:c.305_306delinsAA	NP_683720.2:p.Arg102Gln
NM_148919.4:c.305_306delinsAA MANE Select	NP_683720.2:p.Arg102Gln
NM_004159.5:c.293_294delinsAA	NP_004150.1:p.Arg98Gln