Canonical Allele Identifier: CA462458174

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100866003C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99853775C>A , CM000670.2:g.99853775C>A	GRCh38
NC_000008.10:g.100866003C>A , CM000670.1:g.100866003C>A	GRCh37
NC_000008.9:g.100935179C>A	NCBI36
NG_007098.2:g.845510C>A , LRG_351:g.845510C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10461C>A	ENSP00000507923.1:p.Leu3487=
ENST00000682358.1:n.10531C>A
ENST00000683334.1:c.*6143C>A	ENSP00000507369.1:n.*6143C>A
ENST00000357162.7:c.10386C>A MANE Select	ENSP00000349685.2:p.Leu3462=
ENST00000358544.7:c.10461C>A MANE Plus Clinical	ENSP00000351346.2:p.Leu3487=
ENST00000357162.6:c.10386C>A	ENSP00000349685.2:p.Leu3462=
ENST00000358544.6:c.10461C>A	ENSP00000351346.2:p.Leu3487=
NM_017890.4:c.10461C>A , LRG_351t1:c.10461C>A	NP_060360.3:p.Leu3487=
NM_152564.4:c.10386C>A , LRG_351t2:c.10386C>A	NP_689777.3:p.Leu3462=
XM_005250800.2:c.10461C>A	XP_005250857.1:p.Leu3487=
XM_005250801.3:c.10461C>A	XP_005250858.1:p.Leu3487=
XM_011516848.1:c.10458C>A	XP_011515150.1:p.Leu3486=
XM_011516849.1:c.10383C>A	XP_011515151.1:p.Leu3461=
XM_011516850.1:c.10083C>A	XP_011515152.1:p.Leu3361=
XM_011516851.1:c.7347C>A	XP_011515153.1:p.Leu2449=
XM_011516852.1:c.7347C>A	XP_011515154.1:p.Leu2449=
XM_011516854.1:c.6240C>A	XP_011515156.1:p.Leu2080=
XM_005250800.3:c.10461C>A	XP_005250857.1:p.Leu3487=
XM_005250801.5:c.10461C>A	XP_005250858.1:p.Leu3487=
XM_011516848.2:c.10458C>A	XP_011515150.1:p.Leu3486=
XM_011516849.2:c.10383C>A	XP_011515151.1:p.Leu3461=
XM_011516850.2:c.10083C>A	XP_011515152.1:p.Leu3361=
XM_011516851.2:c.7347C>A	XP_011515153.1:p.Leu2449=
XM_011516852.2:c.7347C>A	XP_011515154.1:p.Leu2449=
XM_011516854.2:c.6240C>A	XP_011515156.1:p.Leu2080=
XM_017013109.1:c.10266C>A	XP_016868598.1:p.Leu3422=
XM_017013111.1:c.7347C>A	XP_016868600.1:p.Leu2449=
XM_017013112.1:c.6018C>A	XP_016868601.1:p.Leu2006=
XM_024447074.1:c.9246C>A	XP_024302842.1:p.Leu3082=
NM_017890.5:c.10461C>A MANE Plus Clinical	NP_060360.3:p.Leu3487=
NM_152564.5:c.10386C>A MANE Select	NP_689777.3:p.Leu3462=