Canonical Allele Identifier: CA3746497

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843868A>G , CM000668.2:g.32843868A>G	GRCh38
NC_000006.11:g.32811645A>G , CM000668.1:g.32811645A>G	GRCh37
NC_000006.10:g.32919623A>G	NCBI36
NG_011759.1:g.15104T>C
NG_028165.1:g.6068T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.150T>C
ENST00000697612.1:n.68T>C
ENST00000374881.3:c.135+411T>C	ENSP00000364015.2:n.135+411T>C
ENST00000374882.8:c.129T>C MANE Select	ENSP00000364016.4:p.Ala43=
ENST00000650411.1:n.690T>C
ENST00000650793.1:n.150T>C
ENST00000374881.2:c.135+411T>C	ENSP00000364015.2:n.135+411T>C
ENST00000374882.7:c.129T>C	ENSP00000364016.3:p.Ala43=
ENST00000395339.7:c.129T>C	ENSP00000378748.3:p.Ala43=
ENST00000484003.1:n.373+411T>C
NM_004159.4:c.135+411T>C	NP_004150.1:n.135+411T>C
NM_148919.3:c.129T>C	NP_683720.2:p.Ala43=
NM_148919.4:c.129T>C MANE Select	NP_683720.2:p.Ala43=
NM_004159.5:c.135+411T>C	NP_004150.1:n.135+411T>C