Canonical Allele Identifier: CA137008119

Gene: PSMB8

Linked Data

• dbSNP Id: rs386699801

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32843015_32843017delinsTGA , CM000668.2:g.32843015_32843017delinsTGA	GRCh38
NC_000006.11:g.32810792_32810794delinsTGA , CM000668.1:g.32810792_32810794delinsTGA	GRCh37
NC_000006.10:g.32918770_32918772delinsTGA	NCBI36
NG_009793.3:g.754_756delinsTCA
NG_028165.1:g.6919_6921delinsTCA
NG_009793.4:g.754_756delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.241_243delinsTCA
ENST00000697612.1:n.919_921delinsTCA
ENST00000374881.3:c.208_210delinsTCA	ENSP00000364015.2:p.Thr70Ser
ENST00000374882.8:c.220_222delinsTCA MANE Select	ENSP00000364016.4:p.Thr74Ser
ENST00000650411.1:n.1541_1543delinsTCA
ENST00000650793.1:n.241_243delinsTCA
ENST00000374881.2:c.208_210delinsTCA	ENSP00000364015.2:p.Thr70Ser
ENST00000374882.7:c.220_222delinsTCA	ENSP00000364016.3:p.Thr74Ser
ENST00000395339.7:c.220_222delinsTCA	ENSP00000378748.3:p.Thr74Ser
ENST00000484003.1:n.446_448delinsTCA
NM_004159.4:c.208_210delinsTCA	NP_004150.1:p.Thr70Ser
NM_148919.3:c.220_222delinsTCA	NP_683720.2:p.Thr74Ser
NM_148919.4:c.220_222delinsTCA MANE Select	NP_683720.2:p.Thr74Ser
NM_004159.5:c.208_210delinsTCA	NP_004150.1:p.Thr70Ser