Canonical Allele Identifier: CA371792161

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100880631T>A (hg19) ; chr8:g.99868403T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99868403T>A , CM000670.2:g.99868403T>A	GRCh38
NC_000008.10:g.100880631T>A , CM000670.1:g.100880631T>A	GRCh37
NC_000008.9:g.100949807T>A	NCBI36
NG_007098.2:g.860138T>A , LRG_351:g.860138T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*499T>A	ENSP00000507923.1:n.*499T>A
ENST00000682358.1:n.11475T>A
ENST00000683334.1:c.*7087T>A	ENSP00000507369.1:n.*7087T>A
ENST00000357162.7:c.11330T>A MANE Select	ENSP00000349685.2:p.Ile3777Asn
ENST00000358544.7:c.11405T>A MANE Plus Clinical	ENSP00000351346.2:p.Ile3802Asn
ENST00000357162.6:c.11330T>A	ENSP00000349685.2:p.Ile3777Asn
ENST00000358544.6:c.11405T>A	ENSP00000351346.2:p.Ile3802Asn
ENST00000493587.1:n.347T>A
NM_017890.4:c.11405T>A , LRG_351t1:c.11405T>A	NP_060360.3:p.Ile3802Asn
NM_152564.4:c.11330T>A , LRG_351t2:c.11330T>A	NP_689777.3:p.Ile3777Asn
XM_005250800.2:c.11405T>A	XP_005250857.1:p.Ile3802Asn
XM_005250801.3:c.11405T>A	XP_005250858.1:p.Ile3802Asn
XM_011516848.1:c.11402T>A	XP_011515150.1:p.Ile3801Asn
XM_011516849.1:c.11327T>A	XP_011515151.1:p.Ile3776Asn
XM_011516850.1:c.11027T>A	XP_011515152.1:p.Ile3676Asn
XM_011516851.1:c.8291T>A	XP_011515153.1:p.Ile2764Asn
XM_011516852.1:c.8291T>A	XP_011515154.1:p.Ile2764Asn
XM_011516854.1:c.7184T>A	XP_011515156.1:p.Ile2395Asn
XM_005250800.3:c.11405T>A	XP_005250857.1:p.Ile3802Asn
XM_005250801.5:c.11405T>A	XP_005250858.1:p.Ile3802Asn
XM_011516848.2:c.11402T>A	XP_011515150.1:p.Ile3801Asn
XM_011516849.2:c.11327T>A	XP_011515151.1:p.Ile3776Asn
XM_011516850.2:c.11027T>A	XP_011515152.1:p.Ile3676Asn
XM_011516851.2:c.8291T>A	XP_011515153.1:p.Ile2764Asn
XM_011516852.2:c.8291T>A	XP_011515154.1:p.Ile2764Asn
XM_011516854.2:c.7184T>A	XP_011515156.1:p.Ile2395Asn
XM_017013109.1:c.11210T>A	XP_016868598.1:p.Ile3737Asn
XM_017013111.1:c.8291T>A	XP_016868600.1:p.Ile2764Asn
XM_017013112.1:c.6962T>A	XP_016868601.1:p.Ile2321Asn
XM_024447074.1:c.10190T>A	XP_024302842.1:p.Ile3397Asn
NM_017890.5:c.11405T>A MANE Plus Clinical	NP_060360.3:p.Ile3802Asn
NM_152564.5:c.11330T>A MANE Select	NP_689777.3:p.Ile3777Asn