Canonical Allele Identifier: CA1619759978

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843006_32843010delinsGGCGA , CM000668.2:g.32843006_32843010delinsGGCGA	GRCh38
NC_000006.11:g.32810783_32810787delinsGGCGA , CM000668.1:g.32810783_32810787delinsGGCGA	GRCh37
NC_000006.10:g.32918761_32918765delinsGGCGA	NCBI36
NG_009793.3:g.761_765delinsTCGCC
NG_028165.1:g.6926_6930delinsTCGCC
NG_009793.4:g.761_765delinsTCGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.248_252delinsTCGCC
ENST00000697612.1:n.926_930delinsTCGCC
ENST00000374881.3:c.215_219delinsTCGCC	ENSP00000364015.2:p.Leu72=
ENST00000374882.8:c.227_231delinsTCGCC MANE Select	ENSP00000364016.4:p.Leu76=
ENST00000650411.1:n.1548_1552delinsTCGCC
ENST00000650793.1:n.248_252delinsTCGCC
ENST00000374881.2:c.215_219delinsTCGCC	ENSP00000364015.2:p.Leu72=
ENST00000374882.7:c.227_231delinsTCGCC	ENSP00000364016.3:p.Leu76=
ENST00000395339.7:c.227_231delinsTCGCC	ENSP00000378748.3:p.Leu76=
ENST00000484003.1:n.453_457delinsTCGCC
NM_004159.4:c.215_219delinsTCGCC	NP_004150.1:p.Leu72=
NM_148919.3:c.227_231delinsTCGCC	NP_683720.2:p.Leu76=
NM_148919.4:c.227_231delinsTCGCC MANE Select	NP_683720.2:p.Leu76=
NM_004159.5:c.215_219delinsTCGCC	NP_004150.1:p.Leu72=