Canonical Allele Identifier: CA137007950

Gene: PSMB8

Linked Data

• ClinVar Variation Id: 653137
• ClinVar RCV Id: RCV003596592
• dbSNP Id: rs371826956

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842772_32842773delinsTT , CM000668.2:g.32842772_32842773delinsTT	GRCh38
NC_000006.11:g.32810549_32810550delinsTT , CM000668.1:g.32810549_32810550delinsTT	GRCh37
NC_000006.10:g.32918527_32918528delinsTT	NCBI36
NG_009793.3:g.998_999delinsAA
NG_028165.1:g.7163_7164delinsAA
NG_009793.4:g.998_999delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.485_486delinsAA
ENST00000697612.1:n.1163_1164delinsAA
ENST00000374881.3:c.294_295delinsAA	ENSP00000364015.2:p.Val99Met
ENST00000374882.8:c.306_307delinsAA MANE Select	ENSP00000364016.4:p.Val103Met
ENST00000650411.1:n.1627_1628delinsAA
ENST00000650793.1:n.485_486delinsAA
ENST00000374881.2:c.294_295delinsAA	ENSP00000364015.2:p.Val99Met
ENST00000374882.7:c.306_307delinsAA	ENSP00000364016.3:p.Val103Met
ENST00000395339.7:c.296-62_296-61delinsAA	ENSP00000378748.3:n.296-62_296-61delinsAA
ENST00000484003.1:n.690_691delinsAA
NM_004159.4:c.294_295delinsAA	NP_004150.1:p.Val99Met
NM_148919.3:c.306_307delinsAA	NP_683720.2:p.Val103Met
NM_148919.4:c.306_307delinsAA MANE Select	NP_683720.2:p.Val103Met
NM_004159.5:c.294_295delinsAA	NP_004150.1:p.Val99Met