Canonical Allele Identifier: CA371792048

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880601A>G (hg19) ; chr8:g.99868373A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868373A>G , CM000670.2:g.99868373A>G	GRCh38
NC_000008.10:g.100880601A>G , CM000670.1:g.100880601A>G	GRCh37
NC_000008.9:g.100949777A>G	NCBI36
NG_007098.2:g.860108A>G , LRG_351:g.860108A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*469A>G	ENSP00000507923.1:n.*469A>G
ENST00000682358.1:n.11445A>G
ENST00000683334.1:c.*7057A>G	ENSP00000507369.1:n.*7057A>G
ENST00000357162.7:c.11300A>G MANE Select	ENSP00000349685.2:p.Lys3767Arg
ENST00000358544.7:c.11375A>G MANE Plus Clinical	ENSP00000351346.2:p.Lys3792Arg
ENST00000357162.6:c.11300A>G	ENSP00000349685.2:p.Lys3767Arg
ENST00000358544.6:c.11375A>G	ENSP00000351346.2:p.Lys3792Arg
ENST00000493587.1:n.317A>G
NM_017890.4:c.11375A>G , LRG_351t1:c.11375A>G	NP_060360.3:p.Lys3792Arg
NM_152564.4:c.11300A>G , LRG_351t2:c.11300A>G	NP_689777.3:p.Lys3767Arg
XM_005250800.2:c.11375A>G	XP_005250857.1:p.Lys3792Arg
XM_005250801.3:c.11375A>G	XP_005250858.1:p.Lys3792Arg
XM_011516848.1:c.11372A>G	XP_011515150.1:p.Lys3791Arg
XM_011516849.1:c.11297A>G	XP_011515151.1:p.Lys3766Arg
XM_011516850.1:c.10997A>G	XP_011515152.1:p.Lys3666Arg
XM_011516851.1:c.8261A>G	XP_011515153.1:p.Lys2754Arg
XM_011516852.1:c.8261A>G	XP_011515154.1:p.Lys2754Arg
XM_011516854.1:c.7154A>G	XP_011515156.1:p.Lys2385Arg
XM_005250800.3:c.11375A>G	XP_005250857.1:p.Lys3792Arg
XM_005250801.5:c.11375A>G	XP_005250858.1:p.Lys3792Arg
XM_011516848.2:c.11372A>G	XP_011515150.1:p.Lys3791Arg
XM_011516849.2:c.11297A>G	XP_011515151.1:p.Lys3766Arg
XM_011516850.2:c.10997A>G	XP_011515152.1:p.Lys3666Arg
XM_011516851.2:c.8261A>G	XP_011515153.1:p.Lys2754Arg
XM_011516852.2:c.8261A>G	XP_011515154.1:p.Lys2754Arg
XM_011516854.2:c.7154A>G	XP_011515156.1:p.Lys2385Arg
XM_017013109.1:c.11180A>G	XP_016868598.1:p.Lys3727Arg
XM_017013111.1:c.8261A>G	XP_016868600.1:p.Lys2754Arg
XM_017013112.1:c.6932A>G	XP_016868601.1:p.Lys2311Arg
XM_024447074.1:c.10160A>G	XP_024302842.1:p.Lys3387Arg
NM_017890.5:c.11375A>G MANE Plus Clinical	NP_060360.3:p.Lys3792Arg
NM_152564.5:c.11300A>G MANE Select	NP_689777.3:p.Lys3767Arg