Canonical Allele Identifier: CA1619759766

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842665_32842669delinsCGCTT , CM000668.2:g.32842665_32842669delinsCGCTT	GRCh38
NC_000006.11:g.32810442_32810446delinsCGCTT , CM000668.1:g.32810442_32810446delinsCGCTT	GRCh37
NC_000006.10:g.32918420_32918424delinsCGCTT	NCBI36
NG_009793.3:g.1102_1106delinsAAGCG
NG_028165.1:g.7267_7271delinsAAGCG
NG_009793.4:g.1102_1106delinsAAGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.589_593delinsAAGCG
ENST00000697612.1:n.1264+3_1264+7delinsAAGCG
ENST00000374881.3:c.395+3_395+7delinsAAGCG	ENSP00000364015.2:n.395+3_395+7delinsAAGCG
ENST00000374882.8:c.407+3_407+7delinsAAGCG MANE Select	ENSP00000364016.4:n.407+3_407+7delinsAAGCG
ENST00000650411.1:n.1728+3_1728+7delinsAAGCG
ENST00000650793.1:n.589_593delinsAAGCG
ENST00000374881.2:c.395+3_395+7delinsAAGCG	ENSP00000364015.2:n.395+3_395+7delinsAAGCG
ENST00000374882.7:c.407+3_407+7delinsAAGCG	ENSP00000364016.3:n.407+3_407+7delinsAAGCG
ENST00000395339.7:c.335+3_335+7delinsAAGCG	ENSP00000378748.3:n.335+3_335+7delinsAAGCG
ENST00000484003.1:n.791+3_791+7delinsAAGCG
NM_004159.4:c.395+3_395+7delinsAAGCG	NP_004150.1:n.395+3_395+7delinsAAGCG
NM_148919.3:c.407+3_407+7delinsAAGCG	NP_683720.2:n.407+3_407+7delinsAAGCG
NM_148919.4:c.407+3_407+7delinsAAGCG MANE Select	NP_683720.2:n.407+3_407+7delinsAAGCG
NM_004159.5:c.395+3_395+7delinsAAGCG	NP_004150.1:n.395+3_395+7delinsAAGCG