Canonical Allele Identifier: CA2711373499
Gene: PSMB8 HGNC NCBI

Linked Data

dbSNP Id: rs2127378850

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32843092_32843093insCATTCCCCGGGGTAAAGCGAGCTCTGGAGATCGC , CM000668.2:g.32843092_32843093insCATTCCCCGGGGTAAAGCGAGCTCTGGAGATCGC GRCh38
NC_000006.11:g.32810869_32810870insCATTCCCCGGGGTAAAGCGAGCTCTGGAGATCGC , CM000668.1:g.32810869_32810870insCATTCCCCGGGGTAAAGCGAGCTCTGGAGATCGC GRCh37
NC_000006.10:g.32918847_32918848insCATTCCCCGGGGTAAAGCGAGCTCTGGAGATCGC NCBI36
NG_009793.3:g.678_679insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
NG_028165.1:g.6843_6844insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
NG_009793.4:g.678_679insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.169-4_169-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
ENST00000697612.1:n.843_844insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
ENST00000374881.3:c.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG ENSP00000364015.2:n.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCG...
ENST00000374882.8:c.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG MANE Select ENSP00000364016.4:n.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCG...
ENST00000650411.1:n.1465_1466insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
ENST00000650793.1:n.169-4_169-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
ENST00000374881.2:c.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG ENSP00000364015.2:n.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCG...
ENST00000374882.7:c.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG ENSP00000364016.3:n.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCG...
ENST00000395339.7:c.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG ENSP00000378748.3:n.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCG...
ENST00000484003.1:n.374-4_374-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG
NM_004159.4:c.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG NP_004150.1:n.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAAT...
NM_148919.3:c.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG NP_683720.2:n.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAAT...
NM_148919.4:c.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG MANE Select NP_683720.2:n.148-4_148-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAAT...
NM_004159.5:c.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAATG NP_004150.1:n.136-4_136-3insGCGATCTCCAGAGCTCGCTTTACCCCGGGGAAT...