Canonical Allele Identifier: CA1619759779
Gene: PSMB8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32842687A= , CM000668.2:g.32842687A= GRCh38
NC_000006.11:g.32810464A= , CM000668.1:g.32810464A= GRCh37
NC_000006.10:g.32918442A= NCBI36
NG_009793.3:g.1084T=
NG_028165.1:g.7249T=
NG_009793.4:g.1084T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650793.2:n.571T=
ENST00000697612.1:n.1249T=
ENST00000374881.3:c.380T= ENSP00000364015.2:p.Leu127=
ENST00000374882.8:c.392T= MANE Select ENSP00000364016.4:p.Leu131=
ENST00000650411.1:n.1713T=
ENST00000650793.1:n.571T=
ENST00000374881.2:c.380T= ENSP00000364015.2:p.Leu127=
ENST00000374882.7:c.392T= ENSP00000364016.3:p.Leu131=
ENST00000395339.7:c.320T= ENSP00000378748.3:p.Leu107=
ENST00000484003.1:n.776T=
NM_004159.4:c.380T= NP_004150.1:p.Leu127=
NM_148919.3:c.392T= NP_683720.2:p.Leu131=
NM_148919.4:c.392T= MANE Select NP_683720.2:p.Leu131=
NM_004159.5:c.380T= NP_004150.1:p.Leu127=