Canonical Allele Identifier: CA2688071646

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99861726-TCCATCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861727_99861732del , CM000670.2:g.99861727_99861732del	GRCh38
NC_000008.10:g.100873955_100873960del , CM000670.1:g.100873955_100873960del	GRCh37
NC_000008.9:g.100943131_100943136del	NCBI36
NG_007098.2:g.853462_853467del , LRG_351:g.853462_853467del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*214-49_*214-44del	ENSP00000507923.1:n.*214-49_*214-44del
ENST00000682358.1:n.11190-49_11190-44del
ENST00000683334.1:c.*6802-49_*6802-44del	ENSP00000507369.1:n.*6802-49_*6802-44del
ENST00000357162.7:c.11045-49_11045-44del MANE Select	ENSP00000349685.2:n.11045-49_11045-44del
ENST00000358544.7:c.11120-49_11120-44del MANE Plus Clinical	ENSP00000351346.2:n.11120-49_11120-44del
ENST00000357162.6:c.11045-49_11045-44del	ENSP00000349685.2:n.11045-49_11045-44del
ENST00000358544.6:c.11120-49_11120-44del	ENSP00000351346.2:n.11120-49_11120-44del
NM_017890.4:c.11120-49_11120-44del , LRG_351t1:c.11120-49_11120-44del	NP_060360.3:n.11120-49_11120-44del
NM_152564.4:c.11045-49_11045-44del , LRG_351t2:c.11045-49_11045-44del	NP_689777.3:n.11045-49_11045-44del
XM_005250800.2:c.11120-49_11120-44del	XP_005250857.1:n.11120-49_11120-44del
XM_005250801.3:c.11120-49_11120-44del	XP_005250858.1:n.11120-49_11120-44del
XM_011516848.1:c.11117-49_11117-44del	XP_011515150.1:n.11117-49_11117-44del
XM_011516849.1:c.11042-49_11042-44del	XP_011515151.1:n.11042-49_11042-44del
XM_011516850.1:c.10742-49_10742-44del	XP_011515152.1:n.10742-49_10742-44del
XM_011516851.1:c.8006-49_8006-44del	XP_011515153.1:n.8006-49_8006-44del
XM_011516852.1:c.8006-49_8006-44del	XP_011515154.1:n.8006-49_8006-44del
XM_011516854.1:c.6899-49_6899-44del	XP_011515156.1:n.6899-49_6899-44del
XM_005250800.3:c.11120-49_11120-44del	XP_005250857.1:n.11120-49_11120-44del
XM_005250801.5:c.11120-49_11120-44del	XP_005250858.1:n.11120-49_11120-44del
XM_011516848.2:c.11117-49_11117-44del	XP_011515150.1:n.11117-49_11117-44del
XM_011516849.2:c.11042-49_11042-44del	XP_011515151.1:n.11042-49_11042-44del
XM_011516850.2:c.10742-49_10742-44del	XP_011515152.1:n.10742-49_10742-44del
XM_011516851.2:c.8006-49_8006-44del	XP_011515153.1:n.8006-49_8006-44del
XM_011516852.2:c.8006-49_8006-44del	XP_011515154.1:n.8006-49_8006-44del
XM_011516854.2:c.6899-49_6899-44del	XP_011515156.1:n.6899-49_6899-44del
XM_017013109.1:c.10925-49_10925-44del	XP_016868598.1:n.10925-49_10925-44del
XM_017013111.1:c.8006-49_8006-44del	XP_016868600.1:n.8006-49_8006-44del
XM_017013112.1:c.6677-49_6677-44del	XP_016868601.1:n.6677-49_6677-44del
XM_024447074.1:c.9905-49_9905-44del	XP_024302842.1:n.9905-49_9905-44del
NM_017890.5:c.11120-49_11120-44del MANE Plus Clinical	NP_060360.3:n.11120-49_11120-44del
NM_152564.5:c.11045-49_11045-44del MANE Select	NP_689777.3:n.11045-49_11045-44del