Canonical Allele Identifier: CA371782679

Gene: VPS13B

Linked Data

• gnomAD v4: 8-99853785-A-G
• MyVariant Identifiers: chr8:g.100866013A>G (hg19) ; chr8:g.99853785A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99853785A>G , CM000670.2:g.99853785A>G	GRCh38
NC_000008.10:g.100866013A>G , CM000670.1:g.100866013A>G	GRCh37
NC_000008.9:g.100935189A>G	NCBI36
NG_007098.2:g.845520A>G , LRG_351:g.845520A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.10471A>G	ENSP00000507923.1:p.Asn3491Asp
ENST00000682358.1:n.10541A>G
ENST00000683334.1:c.*6153A>G	ENSP00000507369.1:n.*6153A>G
ENST00000357162.7:c.10396A>G MANE Select	ENSP00000349685.2:p.Asn3466Asp
ENST00000358544.7:c.10471A>G MANE Plus Clinical	ENSP00000351346.2:p.Asn3491Asp
ENST00000357162.6:c.10396A>G	ENSP00000349685.2:p.Asn3466Asp
ENST00000358544.6:c.10471A>G	ENSP00000351346.2:p.Asn3491Asp
NM_017890.4:c.10471A>G , LRG_351t1:c.10471A>G	NP_060360.3:p.Asn3491Asp
NM_152564.4:c.10396A>G , LRG_351t2:c.10396A>G	NP_689777.3:p.Asn3466Asp
XM_005250800.2:c.10471A>G	XP_005250857.1:p.Asn3491Asp
XM_005250801.3:c.10471A>G	XP_005250858.1:p.Asn3491Asp
XM_011516848.1:c.10468A>G	XP_011515150.1:p.Asn3490Asp
XM_011516849.1:c.10393A>G	XP_011515151.1:p.Asn3465Asp
XM_011516850.1:c.10093A>G	XP_011515152.1:p.Asn3365Asp
XM_011516851.1:c.7357A>G	XP_011515153.1:p.Asn2453Asp
XM_011516852.1:c.7357A>G	XP_011515154.1:p.Asn2453Asp
XM_011516854.1:c.6250A>G	XP_011515156.1:p.Asn2084Asp
XM_005250800.3:c.10471A>G	XP_005250857.1:p.Asn3491Asp
XM_005250801.5:c.10471A>G	XP_005250858.1:p.Asn3491Asp
XM_011516848.2:c.10468A>G	XP_011515150.1:p.Asn3490Asp
XM_011516849.2:c.10393A>G	XP_011515151.1:p.Asn3465Asp
XM_011516850.2:c.10093A>G	XP_011515152.1:p.Asn3365Asp
XM_011516851.2:c.7357A>G	XP_011515153.1:p.Asn2453Asp
XM_011516852.2:c.7357A>G	XP_011515154.1:p.Asn2453Asp
XM_011516854.2:c.6250A>G	XP_011515156.1:p.Asn2084Asp
XM_017013109.1:c.10276A>G	XP_016868598.1:p.Asn3426Asp
XM_017013111.1:c.7357A>G	XP_016868600.1:p.Asn2453Asp
XM_017013112.1:c.6028A>G	XP_016868601.1:p.Asn2010Asp
XM_024447074.1:c.9256A>G	XP_024302842.1:p.Asn3086Asp
NM_017890.5:c.10471A>G MANE Plus Clinical	NP_060360.3:p.Asn3491Asp
NM_152564.5:c.10396A>G MANE Select	NP_689777.3:p.Asn3466Asp