Canonical Allele Identifier: CA371875820

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100789139C>A (hg19) ; chr8:g.99776911C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776911C>A , CM000670.2:g.99776911C>A	GRCh38
NC_000008.10:g.100789139C>A , CM000670.1:g.100789139C>A	GRCh37
NC_000008.9:g.100858315C>A	NCBI36
NG_007098.2:g.768646C>A , LRG_351:g.768646C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7459C>A	ENSP00000507923.1:p.His2487Asn
ENST00000682358.1:n.7529C>A
ENST00000683334.1:c.*3141C>A	ENSP00000507369.1:n.*3141C>A
ENST00000357162.7:c.7384C>A MANE Select	ENSP00000349685.2:p.His2462Asn
ENST00000358544.7:c.7459C>A MANE Plus Clinical	ENSP00000351346.2:p.His2487Asn
ENST00000357162.6:c.7384C>A	ENSP00000349685.2:p.His2462Asn
ENST00000358544.6:c.7459C>A	ENSP00000351346.2:p.His2487Asn
ENST00000518569.1:n.378-1771C>A
NM_017890.4:c.7459C>A , LRG_351t1:c.7459C>A	NP_060360.3:p.His2487Asn
NM_152564.4:c.7384C>A , LRG_351t2:c.7384C>A	NP_689777.3:p.His2462Asn
XM_005250800.2:c.7459C>A	XP_005250857.1:p.His2487Asn
XM_005250801.3:c.7459C>A	XP_005250858.1:p.His2487Asn
XM_011516848.1:c.7456C>A	XP_011515150.1:p.His2486Asn
XM_011516849.1:c.7381C>A	XP_011515151.1:p.His2461Asn
XM_011516850.1:c.7081C>A	XP_011515152.1:p.His2361Asn
XM_011516851.1:c.4345C>A	XP_011515153.1:p.His1449Asn
XM_011516852.1:c.4345C>A	XP_011515154.1:p.His1449Asn
XM_011516853.1:c.7459C>A	XP_011515155.1:p.His2487Asn
XM_011516854.1:c.3238C>A	XP_011515156.1:p.His1080Asn
XR_928446.1:n.1830+5567G>T
XM_005250800.3:c.7459C>A	XP_005250857.1:p.His2487Asn
XM_005250801.5:c.7459C>A	XP_005250858.1:p.His2487Asn
XM_011516848.2:c.7456C>A	XP_011515150.1:p.His2486Asn
XM_011516849.2:c.7381C>A	XP_011515151.1:p.His2461Asn
XM_011516850.2:c.7081C>A	XP_011515152.1:p.His2361Asn
XM_011516851.2:c.4345C>A	XP_011515153.1:p.His1449Asn
XM_011516852.2:c.4345C>A	XP_011515154.1:p.His1449Asn
XM_011516853.2:c.7459C>A	XP_011515155.1:p.His2487Asn
XM_011516854.2:c.3238C>A	XP_011515156.1:p.His1080Asn
XM_017013109.1:c.7264C>A	XP_016868598.1:p.His2422Asn
XM_017013111.1:c.4345C>A	XP_016868600.1:p.His1449Asn
XM_017013112.1:c.3016C>A	XP_016868601.1:p.His1006Asn
XM_024447074.1:c.6244C>A	XP_024302842.1:p.His2082Asn
NM_017890.5:c.7459C>A MANE Plus Clinical	NP_060360.3:p.His2487Asn
NM_152564.5:c.7384C>A MANE Select	NP_689777.3:p.His2462Asn