Canonical Allele Identifier: CA3156712806

Gene: VPS13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99818485G= , CM000670.2:g.99818485G=	GRCh38
NC_000008.10:g.100830713G= , CM000670.1:g.100830713G=	GRCh37
NC_000008.9:g.100899889G=	NCBI36
NG_007098.2:g.810220G= , LRG_351:g.810220G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8471G=	ENSP00000507923.1:p.Trp2824=
ENST00000682358.1:n.8541G=
ENST00000683334.1:c.*4153G=	ENSP00000507369.1:n.*4153G=
ENST00000357162.7:c.8396G= MANE Select	ENSP00000349685.2:p.Trp2799=
ENST00000358544.7:c.8471G= MANE Plus Clinical	ENSP00000351346.2:p.Trp2824=
ENST00000357162.6:c.8396G=	ENSP00000349685.2:p.Trp2799=
ENST00000358544.6:c.8471G=	ENSP00000351346.2:p.Trp2824=
NM_017890.4:c.8471G= , LRG_351t1:c.8471G=	NP_060360.3:p.Trp2824=
NM_152564.4:c.8396G= , LRG_351t2:c.8396G=	NP_689777.3:p.Trp2799=
XM_005250800.2:c.8471G=	XP_005250857.1:p.Trp2824=
XM_005250801.3:c.8471G=	XP_005250858.1:p.Trp2824=
XM_011516848.1:c.8468G=	XP_011515150.1:p.Trp2823=
XM_011516849.1:c.8393G=	XP_011515151.1:p.Trp2798=
XM_011516850.1:c.8093G=	XP_011515152.1:p.Trp2698=
XM_011516851.1:c.5357G=	XP_011515153.1:p.Trp1786=
XM_011516852.1:c.5357G=	XP_011515154.1:p.Trp1786=
XM_011516854.1:c.4250G=	XP_011515156.1:p.Trp1417=
XM_005250800.3:c.8471G=	XP_005250857.1:p.Trp2824=
XM_005250801.5:c.8471G=	XP_005250858.1:p.Trp2824=
XM_011516848.2:c.8468G=	XP_011515150.1:p.Trp2823=
XM_011516849.2:c.8393G=	XP_011515151.1:p.Trp2798=
XM_011516850.2:c.8093G=	XP_011515152.1:p.Trp2698=
XM_011516851.2:c.5357G=	XP_011515153.1:p.Trp1786=
XM_011516852.2:c.5357G=	XP_011515154.1:p.Trp1786=
XM_011516854.2:c.4250G=	XP_011515156.1:p.Trp1417=
XM_017013109.1:c.8276G=	XP_016868598.1:p.Trp2759=
XM_017013111.1:c.5357G=	XP_016868600.1:p.Trp1786=
XM_017013112.1:c.4028G=	XP_016868601.1:p.Trp1343=
XM_024447074.1:c.7256G=	XP_024302842.1:p.Trp2419=
NM_017890.5:c.8471G= MANE Plus Clinical	NP_060360.3:p.Trp2824=
NM_152564.5:c.8396G= MANE Select	NP_689777.3:p.Trp2799=