Canonical Allele Identifier: CA371791728

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880526C>A (hg19) ; chr8:g.99868298C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868298C>A , CM000670.2:g.99868298C>A	GRCh38
NC_000008.10:g.100880526C>A , CM000670.1:g.100880526C>A	GRCh37
NC_000008.9:g.100949702C>A	NCBI36
NG_007098.2:g.860033C>A , LRG_351:g.860033C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682153.1:c.*394C>A	ENSP00000507923.1:n.*394C>A
ENST00000682358.1:n.11370C>A
ENST00000683334.1:c.*6982C>A	ENSP00000507369.1:n.*6982C>A
ENST00000357162.7:c.11225C>A MANE Select	ENSP00000349685.2:p.Ala3742Asp
ENST00000358544.7:c.11300C>A MANE Plus Clinical	ENSP00000351346.2:p.Ala3767Asp
ENST00000357162.6:c.11225C>A	ENSP00000349685.2:p.Ala3742Asp
ENST00000358544.6:c.11300C>A	ENSP00000351346.2:p.Ala3767Asp
ENST00000493587.1:n.242C>A
NM_017890.4:c.11300C>A , LRG_351t1:c.11300C>A	NP_060360.3:p.Ala3767Asp
NM_152564.4:c.11225C>A , LRG_351t2:c.11225C>A	NP_689777.3:p.Ala3742Asp
XM_005250800.2:c.11300C>A	XP_005250857.1:p.Ala3767Asp
XM_005250801.3:c.11300C>A	XP_005250858.1:p.Ala3767Asp
XM_011516848.1:c.11297C>A	XP_011515150.1:p.Ala3766Asp
XM_011516849.1:c.11222C>A	XP_011515151.1:p.Ala3741Asp
XM_011516850.1:c.10922C>A	XP_011515152.1:p.Ala3641Asp
XM_011516851.1:c.8186C>A	XP_011515153.1:p.Ala2729Asp
XM_011516852.1:c.8186C>A	XP_011515154.1:p.Ala2729Asp
XM_011516854.1:c.7079C>A	XP_011515156.1:p.Ala2360Asp
XM_005250800.3:c.11300C>A	XP_005250857.1:p.Ala3767Asp
XM_005250801.5:c.11300C>A	XP_005250858.1:p.Ala3767Asp
XM_011516848.2:c.11297C>A	XP_011515150.1:p.Ala3766Asp
XM_011516849.2:c.11222C>A	XP_011515151.1:p.Ala3741Asp
XM_011516850.2:c.10922C>A	XP_011515152.1:p.Ala3641Asp
XM_011516851.2:c.8186C>A	XP_011515153.1:p.Ala2729Asp
XM_011516852.2:c.8186C>A	XP_011515154.1:p.Ala2729Asp
XM_011516854.2:c.7079C>A	XP_011515156.1:p.Ala2360Asp
XM_017013109.1:c.11105C>A	XP_016868598.1:p.Ala3702Asp
XM_017013111.1:c.8186C>A	XP_016868600.1:p.Ala2729Asp
XM_017013112.1:c.6857C>A	XP_016868601.1:p.Ala2286Asp
XM_024447074.1:c.10085C>A	XP_024302842.1:p.Ala3362Asp
NM_017890.5:c.11300C>A MANE Plus Clinical	NP_060360.3:p.Ala3767Asp
NM_152564.5:c.11225C>A MANE Select	NP_689777.3:p.Ala3742Asp