Canonical Allele Identifier: CA2688072649

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99868160-GTAGTAAAGACC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868162_99868172del , CM000670.2:g.99868162_99868172del	GRCh38
NC_000008.10:g.100880390_100880400del , CM000670.1:g.100880390_100880400del	GRCh37
NC_000008.9:g.100949566_100949576del	NCBI36
NG_007098.2:g.859897_859907del , LRG_351:g.859897_859907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*385-127_*385-117del	ENSP00000507923.1:n.*385-127_*385-117del
ENST00000682358.1:n.11361-127_11361-117del
ENST00000683334.1:c.*6973-127_*6973-117del	ENSP00000507369.1:n.*6973-127_*6973-117del
ENST00000357162.7:c.11216-127_11216-117del MANE Select	ENSP00000349685.2:n.11216-127_11216-117del
ENST00000358544.7:c.11291-127_11291-117del MANE Plus Clinical	ENSP00000351346.2:n.11291-127_11291-117del
ENST00000357162.6:c.11216-127_11216-117del	ENSP00000349685.2:n.11216-127_11216-117del
ENST00000358544.6:c.11291-127_11291-117del	ENSP00000351346.2:n.11291-127_11291-117del
ENST00000493587.1:n.106_116del
NM_017890.4:c.11291-127_11291-117del , LRG_351t1:c.11291-127_11291-117del	NP_060360.3:n.11291-127_11291-117del
NM_152564.4:c.11216-127_11216-117del , LRG_351t2:c.11216-127_11216-117del	NP_689777.3:n.11216-127_11216-117del
XM_005250800.2:c.11291-127_11291-117del	XP_005250857.1:n.11291-127_11291-117del
XM_005250801.3:c.11291-127_11291-117del	XP_005250858.1:n.11291-127_11291-117del
XM_011516848.1:c.11288-127_11288-117del	XP_011515150.1:n.11288-127_11288-117del
XM_011516849.1:c.11213-127_11213-117del	XP_011515151.1:n.11213-127_11213-117del
XM_011516850.1:c.10913-127_10913-117del	XP_011515152.1:n.10913-127_10913-117del
XM_011516851.1:c.8177-127_8177-117del	XP_011515153.1:n.8177-127_8177-117del
XM_011516852.1:c.8177-127_8177-117del	XP_011515154.1:n.8177-127_8177-117del
XM_011516854.1:c.7070-127_7070-117del	XP_011515156.1:n.7070-127_7070-117del
XM_005250800.3:c.11291-127_11291-117del	XP_005250857.1:n.11291-127_11291-117del
XM_005250801.5:c.11291-127_11291-117del	XP_005250858.1:n.11291-127_11291-117del
XM_011516848.2:c.11288-127_11288-117del	XP_011515150.1:n.11288-127_11288-117del
XM_011516849.2:c.11213-127_11213-117del	XP_011515151.1:n.11213-127_11213-117del
XM_011516850.2:c.10913-127_10913-117del	XP_011515152.1:n.10913-127_10913-117del
XM_011516851.2:c.8177-127_8177-117del	XP_011515153.1:n.8177-127_8177-117del
XM_011516852.2:c.8177-127_8177-117del	XP_011515154.1:n.8177-127_8177-117del
XM_011516854.2:c.7070-127_7070-117del	XP_011515156.1:n.7070-127_7070-117del
XM_017013109.1:c.11096-127_11096-117del	XP_016868598.1:n.11096-127_11096-117del
XM_017013111.1:c.8177-127_8177-117del	XP_016868600.1:n.8177-127_8177-117del
XM_017013112.1:c.6848-127_6848-117del	XP_016868601.1:n.6848-127_6848-117del
XM_024447074.1:c.10076-127_10076-117del	XP_024302842.1:n.10076-127_10076-117del
NM_017890.5:c.11291-127_11291-117del MANE Plus Clinical	NP_060360.3:n.11291-127_11291-117del
NM_152564.5:c.11216-127_11216-117del MANE Select	NP_689777.3:n.11216-127_11216-117del