Canonical Allele Identifier: CA1619759763

Gene: PSMB8

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32842664_32842665delinsTC , CM000668.2:g.32842664_32842665delinsTC	GRCh38
NC_000006.11:g.32810441_32810442delinsTC , CM000668.1:g.32810441_32810442delinsTC	GRCh37
NC_000006.10:g.32918419_32918420delinsTC	NCBI36
NG_009793.3:g.1106_1107delinsGA
NG_028165.1:g.7271_7272delinsGA
NG_009793.4:g.1106_1107delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650793.2:n.593_594delinsGA
ENST00000697612.1:n.1264+7_1264+8delinsGA
ENST00000374881.3:c.395+7_395+8delinsGA	ENSP00000364015.2:n.395+7_395+8delinsGA
ENST00000374882.8:c.407+7_407+8delinsGA MANE Select	ENSP00000364016.4:n.407+7_407+8delinsGA
ENST00000650411.1:n.1728+7_1728+8delinsGA
ENST00000650793.1:n.593_594delinsGA
ENST00000374881.2:c.395+7_395+8delinsGA	ENSP00000364015.2:n.395+7_395+8delinsGA
ENST00000374882.7:c.407+7_407+8delinsGA	ENSP00000364016.3:n.407+7_407+8delinsGA
ENST00000395339.7:c.335+7_335+8delinsGA	ENSP00000378748.3:n.335+7_335+8delinsGA
ENST00000484003.1:n.791+7_791+8delinsGA
NM_004159.4:c.395+7_395+8delinsGA	NP_004150.1:n.395+7_395+8delinsGA
NM_148919.3:c.407+7_407+8delinsGA	NP_683720.2:n.407+7_407+8delinsGA
NM_148919.4:c.407+7_407+8delinsGA MANE Select	NP_683720.2:n.407+7_407+8delinsGA
NM_004159.5:c.395+7_395+8delinsGA	NP_004150.1:n.395+7_395+8delinsGA