Canonical Allele Identifier: CA2688071226

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99835856-A-ATACG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835856_99835857insTACG , CM000670.2:g.99835856_99835857insTACG	GRCh38
NC_000008.10:g.100848084_100848085insTACG , CM000670.1:g.100848084_100848085insTACG	GRCh37
NC_000008.9:g.100917260_100917261insTACG	NCBI36
NG_007098.2:g.827591_827592insTACG , LRG_351:g.827591_827592insTACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10017+118_10017+119insTACG	ENSP00000507923.1:n.10017+118_10017+119insTACG
ENST00000682358.1:n.10087+118_10087+119insTACG
ENST00000683334.1:c.*5699+118_*5699+119insTACG	ENSP00000507369.1:n.*5699+118_*5699+119insTACG
ENST00000357162.7:c.9942+118_9942+119insTACG MANE Select	ENSP00000349685.2:n.9942+118_9942+119insTACG
ENST00000358544.7:c.10017+118_10017+119insTACG MANE Plus Clinical	ENSP00000351346.2:n.10017+118_10017+119insTACG
ENST00000357162.6:c.9942+118_9942+119insTACG	ENSP00000349685.2:n.9942+118_9942+119insTACG
ENST00000358544.6:c.10017+118_10017+119insTACG	ENSP00000351346.2:n.10017+118_10017+119insTACG
NM_017890.4:c.10017+118_10017+119insTACG , LRG_351t1:c.10017+118_10017+119insTACG	NP_060360.3:n.10017+118_10017+119insTACG
NM_152564.4:c.9942+118_9942+119insTACG , LRG_351t2:c.9942+118_9942+119insTACG	NP_689777.3:n.9942+118_9942+119insTACG
XM_005250800.2:c.10017+118_10017+119insTACG	XP_005250857.1:n.10017+118_10017+119insTACG
XM_005250801.3:c.10017+118_10017+119insTACG	XP_005250858.1:n.10017+118_10017+119insTACG
XM_011516848.1:c.10014+118_10014+119insTACG	XP_011515150.1:n.10014+118_10014+119insTACG
XM_011516849.1:c.9939+118_9939+119insTACG	XP_011515151.1:n.9939+118_9939+119insTACG
XM_011516850.1:c.9639+118_9639+119insTACG	XP_011515152.1:n.9639+118_9639+119insTACG
XM_011516851.1:c.6903+118_6903+119insTACG	XP_011515153.1:n.6903+118_6903+119insTACG
XM_011516852.1:c.6903+118_6903+119insTACG	XP_011515154.1:n.6903+118_6903+119insTACG
XM_011516854.1:c.5796+118_5796+119insTACG	XP_011515156.1:n.5796+118_5796+119insTACG
XM_005250800.3:c.10017+118_10017+119insTACG	XP_005250857.1:n.10017+118_10017+119insTACG
XM_005250801.5:c.10017+118_10017+119insTACG	XP_005250858.1:n.10017+118_10017+119insTACG
XM_011516848.2:c.10014+118_10014+119insTACG	XP_011515150.1:n.10014+118_10014+119insTACG
XM_011516849.2:c.9939+118_9939+119insTACG	XP_011515151.1:n.9939+118_9939+119insTACG
XM_011516850.2:c.9639+118_9639+119insTACG	XP_011515152.1:n.9639+118_9639+119insTACG
XM_011516851.2:c.6903+118_6903+119insTACG	XP_011515153.1:n.6903+118_6903+119insTACG
XM_011516852.2:c.6903+118_6903+119insTACG	XP_011515154.1:n.6903+118_6903+119insTACG
XM_011516854.2:c.5796+118_5796+119insTACG	XP_011515156.1:n.5796+118_5796+119insTACG
XM_017013109.1:c.9822+118_9822+119insTACG	XP_016868598.1:n.9822+118_9822+119insTACG
XM_017013111.1:c.6903+118_6903+119insTACG	XP_016868600.1:n.6903+118_6903+119insTACG
XM_017013112.1:c.5574+118_5574+119insTACG	XP_016868601.1:n.5574+118_5574+119insTACG
XM_024447074.1:c.8802+118_8802+119insTACG	XP_024302842.1:n.8802+118_8802+119insTACG
NM_017890.5:c.10017+118_10017+119insTACG MANE Plus Clinical	NP_060360.3:n.10017+118_10017+119insTACG
NM_152564.5:c.9942+118_9942+119insTACG MANE Select	NP_689777.3:n.9942+118_9942+119insTACG