Canonical Allele Identifier: CA137007625

Gene: PSMB8

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842071G>C , CM000668.2:g.32842071G>C	GRCh38
NC_000006.11:g.32809848G>C , CM000668.1:g.32809848G>C	GRCh37
NC_000006.10:g.32917826G>C	NCBI36
NG_009793.3:g.1700C>G
NG_028165.1:g.7865C>G
NG_009793.4:g.1700C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.1187C>G
ENST00000697612.1:n.1394+63C>G
ENST00000374881.3:c.525+63C>G	ENSP00000364015.2:n.525+63C>G
ENST00000374882.8:c.537+63C>G MANE Select	ENSP00000364016.4:n.537+63C>G
ENST00000650411.1:n.1858+63C>G
ENST00000650793.1:n.1187C>G
ENST00000374881.2:c.525+63C>G	ENSP00000364015.2:n.525+63C>G
ENST00000374882.7:c.537+63C>G	ENSP00000364016.3:n.537+63C>G
ENST00000395339.7:c.465+63C>G	ENSP00000378748.3:n.465+63C>G
ENST00000484003.1:n.921+63C>G
NM_004159.4:c.525+63C>G	NP_004150.1:n.525+63C>G
NM_148919.3:c.537+63C>G	NP_683720.2:n.537+63C>G
NM_148919.4:c.537+63C>G MANE Select	NP_683720.2:n.537+63C>G
NM_004159.5:c.525+63C>G	NP_004150.1:n.525+63C>G