Canonical Allele Identifier: CA1619759834

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842773_32842774delinsCC , CM000668.2:g.32842773_32842774delinsCC	GRCh38
NC_000006.11:g.32810550_32810551delinsCC , CM000668.1:g.32810550_32810551delinsCC	GRCh37
NC_000006.10:g.32918528_32918529delinsCC	NCBI36
NG_009793.3:g.997_998delinsGG
NG_028165.1:g.7162_7163delinsGG
NG_009793.4:g.997_998delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.484_485delinsGG
ENST00000697612.1:n.1162_1163delinsGG
ENST00000374881.3:c.293_294delinsGG	ENSP00000364015.2:p.Arg98=
ENST00000374882.8:c.305_306delinsGG MANE Select	ENSP00000364016.4:p.Arg102=
ENST00000650411.1:n.1626_1627delinsGG
ENST00000650793.1:n.484_485delinsGG
ENST00000374881.2:c.293_294delinsGG	ENSP00000364015.2:p.Arg98=
ENST00000374882.7:c.305_306delinsGG	ENSP00000364016.3:p.Arg102=
ENST00000395339.7:c.296-63_296-62delinsGG	ENSP00000378748.3:n.296-63_296-62delinsGG
ENST00000484003.1:n.689_690delinsGG
NM_004159.4:c.293_294delinsGG	NP_004150.1:p.Arg98=
NM_148919.3:c.305_306delinsGG	NP_683720.2:p.Arg102=
NM_148919.4:c.305_306delinsGG MANE Select	NP_683720.2:p.Arg102=
NM_004159.5:c.293_294delinsGG	NP_004150.1:p.Arg98=