Canonical Allele Identifier: CA371875883

Gene: VPS13B

Linked Data

• COSMIC: COSM748160 ; COSM748161
• MyVariant Identifiers: chr8:g.100789166C>A (hg19) ; chr8:g.99776938C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776938C>A , CM000670.2:g.99776938C>A	GRCh38
NC_000008.10:g.100789166C>A , CM000670.1:g.100789166C>A	GRCh37
NC_000008.9:g.100858342C>A	NCBI36
NG_007098.2:g.768673C>A , LRG_351:g.768673C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7486C>A	ENSP00000507923.1:p.Leu2496Ile
ENST00000682358.1:n.7556C>A
ENST00000683334.1:c.*3168C>A	ENSP00000507369.1:n.*3168C>A
ENST00000357162.7:c.7411C>A MANE Select	ENSP00000349685.2:p.Leu2471Ile
ENST00000358544.7:c.7486C>A MANE Plus Clinical	ENSP00000351346.2:p.Leu2496Ile
ENST00000357162.6:c.7411C>A	ENSP00000349685.2:p.Leu2471Ile
ENST00000358544.6:c.7486C>A	ENSP00000351346.2:p.Leu2496Ile
ENST00000518569.1:n.378-1744C>A
NM_017890.4:c.7486C>A , LRG_351t1:c.7486C>A	NP_060360.3:p.Leu2496Ile
NM_152564.4:c.7411C>A , LRG_351t2:c.7411C>A	NP_689777.3:p.Leu2471Ile
XM_005250800.2:c.7486C>A	XP_005250857.1:p.Leu2496Ile
XM_005250801.3:c.7486C>A	XP_005250858.1:p.Leu2496Ile
XM_011516848.1:c.7483C>A	XP_011515150.1:p.Leu2495Ile
XM_011516849.1:c.7408C>A	XP_011515151.1:p.Leu2470Ile
XM_011516850.1:c.7108C>A	XP_011515152.1:p.Leu2370Ile
XM_011516851.1:c.4372C>A	XP_011515153.1:p.Leu1458Ile
XM_011516852.1:c.4372C>A	XP_011515154.1:p.Leu1458Ile
XM_011516853.1:c.7486C>A	XP_011515155.1:p.Leu2496Ile
XM_011516854.1:c.3265C>A	XP_011515156.1:p.Leu1089Ile
XR_928446.1:n.1830+5540G>T
XM_005250800.3:c.7486C>A	XP_005250857.1:p.Leu2496Ile
XM_005250801.5:c.7486C>A	XP_005250858.1:p.Leu2496Ile
XM_011516848.2:c.7483C>A	XP_011515150.1:p.Leu2495Ile
XM_011516849.2:c.7408C>A	XP_011515151.1:p.Leu2470Ile
XM_011516850.2:c.7108C>A	XP_011515152.1:p.Leu2370Ile
XM_011516851.2:c.4372C>A	XP_011515153.1:p.Leu1458Ile
XM_011516852.2:c.4372C>A	XP_011515154.1:p.Leu1458Ile
XM_011516853.2:c.7486C>A	XP_011515155.1:p.Leu2496Ile
XM_011516854.2:c.3265C>A	XP_011515156.1:p.Leu1089Ile
XM_017013109.1:c.7291C>A	XP_016868598.1:p.Leu2431Ile
XM_017013111.1:c.4372C>A	XP_016868600.1:p.Leu1458Ile
XM_017013112.1:c.3043C>A	XP_016868601.1:p.Leu1015Ile
XM_024447074.1:c.6271C>A	XP_024302842.1:p.Leu2091Ile
NM_017890.5:c.7486C>A MANE Plus Clinical	NP_060360.3:p.Leu2496Ile
NM_152564.5:c.7411C>A MANE Select	NP_689777.3:p.Leu2471Ile