Canonical Allele Identifier: CA371790160

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.99861751del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861751del , CM000670.2:g.99861751del	GRCh38
NC_000008.10:g.100873979del , CM000670.1:g.100873979del	GRCh37
NC_000008.9:g.100943155del	NCBI36
NG_007098.2:g.853486del , LRG_351:g.853486del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*214-25del	ENSP00000507923.1:n.*214-25del
ENST00000682358.1:n.11190-25del
ENST00000683334.1:c.*6802-25del	ENSP00000507369.1:n.*6802-25del
ENST00000357162.7:c.11045-25del MANE Select	ENSP00000349685.2:n.11045-25del
ENST00000358544.7:c.11120-25del MANE Plus Clinical	ENSP00000351346.2:n.11120-25del
ENST00000357162.6:c.11045-25del	ENSP00000349685.2:n.11045-25del
ENST00000358544.6:c.11120-25del	ENSP00000351346.2:n.11120-25del
NM_017890.4:c.11120-25del , LRG_351t1:c.11120-25del	NP_060360.3:n.11120-25del
NM_152564.4:c.11045-25del , LRG_351t2:c.11045-25del	NP_689777.3:n.11045-25del
XM_005250800.2:c.11120-25del	XP_005250857.1:n.11120-25del
XM_005250801.3:c.11120-25del	XP_005250858.1:n.11120-25del
XM_011516848.1:c.11117-25del	XP_011515150.1:n.11117-25del
XM_011516849.1:c.11042-25del	XP_011515151.1:n.11042-25del
XM_011516850.1:c.10742-25del	XP_011515152.1:n.10742-25del
XM_011516851.1:c.8006-25del	XP_011515153.1:n.8006-25del
XM_011516852.1:c.8006-25del	XP_011515154.1:n.8006-25del
XM_011516854.1:c.6899-25del	XP_011515156.1:n.6899-25del
XM_005250800.3:c.11120-25del	XP_005250857.1:n.11120-25del
XM_005250801.5:c.11120-25del	XP_005250858.1:n.11120-25del
XM_011516848.2:c.11117-25del	XP_011515150.1:n.11117-25del
XM_011516849.2:c.11042-25del	XP_011515151.1:n.11042-25del
XM_011516850.2:c.10742-25del	XP_011515152.1:n.10742-25del
XM_011516851.2:c.8006-25del	XP_011515153.1:n.8006-25del
XM_011516852.2:c.8006-25del	XP_011515154.1:n.8006-25del
XM_011516854.2:c.6899-25del	XP_011515156.1:n.6899-25del
XM_017013109.1:c.10925-25del	XP_016868598.1:n.10925-25del
XM_017013111.1:c.8006-25del	XP_016868600.1:n.8006-25del
XM_017013112.1:c.6677-25del	XP_016868601.1:n.6677-25del
XM_024447074.1:c.9905-25del	XP_024302842.1:n.9905-25del
NM_017890.5:c.11120-25del MANE Plus Clinical	NP_060360.3:n.11120-25del
NM_152564.5:c.11045-25del MANE Select	NP_689777.3:n.11045-25del