Canonical Allele Identifier: CA918325991

Gene: VPS13B

Linked Data

• dbSNP Id: rs1563517957
• gnomAD v4: 8-99868258-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868260_99868261dup , CM000670.2:g.99868260_99868261dup	GRCh38
NC_000008.10:g.100880488_100880489dup , CM000670.1:g.100880488_100880489dup	GRCh37
NC_000008.9:g.100949664_100949665dup	NCBI36
NG_007098.2:g.859995_859996dup , LRG_351:g.859995_859996dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*385-29_*385-28dup	ENSP00000507923.1:n.*385-29_*385-28dup
ENST00000682358.1:n.11361-29_11361-28dup
ENST00000683334.1:c.*6973-29_*6973-28dup	ENSP00000507369.1:n.*6973-29_*6973-28dup
ENST00000357162.7:c.11216-29_11216-28dup MANE Select	ENSP00000349685.2:n.11216-29_11216-28dup
ENST00000358544.7:c.11291-29_11291-28dup MANE Plus Clinical	ENSP00000351346.2:n.11291-29_11291-28dup
ENST00000357162.6:c.11216-29_11216-28dup	ENSP00000349685.2:n.11216-29_11216-28dup
ENST00000358544.6:c.11291-29_11291-28dup	ENSP00000351346.2:n.11291-29_11291-28dup
ENST00000493587.1:n.204_205dup
NM_017890.4:c.11291-29_11291-28dup , LRG_351t1:c.11291-29_11291-28dup	NP_060360.3:n.11291-29_11291-28dup
NM_152564.4:c.11216-29_11216-28dup , LRG_351t2:c.11216-29_11216-28dup	NP_689777.3:n.11216-29_11216-28dup
XM_005250800.2:c.11291-29_11291-28dup	XP_005250857.1:n.11291-29_11291-28dup
XM_005250801.3:c.11291-29_11291-28dup	XP_005250858.1:n.11291-29_11291-28dup
XM_011516848.1:c.11288-29_11288-28dup	XP_011515150.1:n.11288-29_11288-28dup
XM_011516849.1:c.11213-29_11213-28dup	XP_011515151.1:n.11213-29_11213-28dup
XM_011516850.1:c.10913-29_10913-28dup	XP_011515152.1:n.10913-29_10913-28dup
XM_011516851.1:c.8177-29_8177-28dup	XP_011515153.1:n.8177-29_8177-28dup
XM_011516852.1:c.8177-29_8177-28dup	XP_011515154.1:n.8177-29_8177-28dup
XM_011516854.1:c.7070-29_7070-28dup	XP_011515156.1:n.7070-29_7070-28dup
XM_005250800.3:c.11291-29_11291-28dup	XP_005250857.1:n.11291-29_11291-28dup
XM_005250801.5:c.11291-29_11291-28dup	XP_005250858.1:n.11291-29_11291-28dup
XM_011516848.2:c.11288-29_11288-28dup	XP_011515150.1:n.11288-29_11288-28dup
XM_011516849.2:c.11213-29_11213-28dup	XP_011515151.1:n.11213-29_11213-28dup
XM_011516850.2:c.10913-29_10913-28dup	XP_011515152.1:n.10913-29_10913-28dup
XM_011516851.2:c.8177-29_8177-28dup	XP_011515153.1:n.8177-29_8177-28dup
XM_011516852.2:c.8177-29_8177-28dup	XP_011515154.1:n.8177-29_8177-28dup
XM_011516854.2:c.7070-29_7070-28dup	XP_011515156.1:n.7070-29_7070-28dup
XM_017013109.1:c.11096-29_11096-28dup	XP_016868598.1:n.11096-29_11096-28dup
XM_017013111.1:c.8177-29_8177-28dup	XP_016868600.1:n.8177-29_8177-28dup
XM_017013112.1:c.6848-29_6848-28dup	XP_016868601.1:n.6848-29_6848-28dup
XM_024447074.1:c.10076-29_10076-28dup	XP_024302842.1:n.10076-29_10076-28dup
NM_017890.5:c.11291-29_11291-28dup MANE Plus Clinical	NP_060360.3:n.11291-29_11291-28dup
NM_152564.5:c.11216-29_11216-28dup MANE Select	NP_689777.3:n.11216-29_11216-28dup