Canonical Allele Identifier: CA4824196

Gene: VPS13B

Linked Data

• ClinVar Variation Id: 2044319
• ClinVar RCV Id: RCV002903601
• dbSNP Id: rs771677434
• ExAC: 8:100789106 G / A
• gnomAD v2: 8-100789106-G-A
• gnomAD v3: 8-99776878-G-A
• gnomAD v4: 8-99776878-G-A
• MyVariant Identifiers: chr8:g.100789106G>A (hg19) ; chr8:g.99776878G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776878G>A , CM000670.2:g.99776878G>A	GRCh38
NC_000008.10:g.100789106G>A , CM000670.1:g.100789106G>A	GRCh37
NC_000008.9:g.100858282G>A	NCBI36
NG_007098.2:g.768613G>A , LRG_351:g.768613G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.7426G>A	ENSP00000507923.1:p.Val2476Ile
ENST00000682358.1:n.7496G>A
ENST00000683334.1:c.*3108G>A	ENSP00000507369.1:n.*3108G>A
ENST00000357162.7:c.7351G>A MANE Select	ENSP00000349685.2:p.Val2451Ile
ENST00000358544.7:c.7426G>A MANE Plus Clinical	ENSP00000351346.2:p.Val2476Ile
ENST00000357162.6:c.7351G>A	ENSP00000349685.2:p.Val2451Ile
ENST00000358544.6:c.7426G>A	ENSP00000351346.2:p.Val2476Ile
ENST00000518569.1:n.378-1804G>A
NM_017890.4:c.7426G>A , LRG_351t1:c.7426G>A	NP_060360.3:p.Val2476Ile
NM_152564.4:c.7351G>A , LRG_351t2:c.7351G>A	NP_689777.3:p.Val2451Ile
XM_005250800.2:c.7426G>A	XP_005250857.1:p.Val2476Ile
XM_005250801.3:c.7426G>A	XP_005250858.1:p.Val2476Ile
XM_011516848.1:c.7423G>A	XP_011515150.1:p.Val2475Ile
XM_011516849.1:c.7348G>A	XP_011515151.1:p.Val2450Ile
XM_011516850.1:c.7048G>A	XP_011515152.1:p.Val2350Ile
XM_011516851.1:c.4312G>A	XP_011515153.1:p.Val1438Ile
XM_011516852.1:c.4312G>A	XP_011515154.1:p.Val1438Ile
XM_011516853.1:c.7426G>A	XP_011515155.1:p.Val2476Ile
XM_011516854.1:c.3205G>A	XP_011515156.1:p.Val1069Ile
XR_928446.1:n.1830+5600C>T
XM_005250800.3:c.7426G>A	XP_005250857.1:p.Val2476Ile
XM_005250801.5:c.7426G>A	XP_005250858.1:p.Val2476Ile
XM_011516848.2:c.7423G>A	XP_011515150.1:p.Val2475Ile
XM_011516849.2:c.7348G>A	XP_011515151.1:p.Val2450Ile
XM_011516850.2:c.7048G>A	XP_011515152.1:p.Val2350Ile
XM_011516851.2:c.4312G>A	XP_011515153.1:p.Val1438Ile
XM_011516852.2:c.4312G>A	XP_011515154.1:p.Val1438Ile
XM_011516853.2:c.7426G>A	XP_011515155.1:p.Val2476Ile
XM_011516854.2:c.3205G>A	XP_011515156.1:p.Val1069Ile
XM_017013109.1:c.7231G>A	XP_016868598.1:p.Val2411Ile
XM_017013111.1:c.4312G>A	XP_016868600.1:p.Val1438Ile
XM_017013112.1:c.2983G>A	XP_016868601.1:p.Val995Ile
XM_024447074.1:c.6211G>A	XP_024302842.1:p.Val2071Ile
NM_017890.5:c.7426G>A MANE Plus Clinical	NP_060360.3:p.Val2476Ile
NM_152564.5:c.7351G>A MANE Select	NP_689777.3:p.Val2451Ile