Canonical Allele Identifier: CA371784763

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100847929G>C (hg19) ; chr8:g.99835701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99835701G>C , CM000670.2:g.99835701G>C	GRCh38
NC_000008.10:g.100847929G>C , CM000670.1:g.100847929G>C	GRCh37
NC_000008.9:g.100917105G>C	NCBI36
NG_007098.2:g.827436G>C , LRG_351:g.827436G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.9980G>C	ENSP00000507923.1:p.Trp3327Ser
ENST00000682358.1:n.10050G>C
ENST00000683334.1:c.*5662G>C	ENSP00000507369.1:n.*5662G>C
ENST00000357162.7:c.9905G>C MANE Select	ENSP00000349685.2:p.Trp3302Ser
ENST00000358544.7:c.9980G>C MANE Plus Clinical	ENSP00000351346.2:p.Trp3327Ser
ENST00000357162.6:c.9905G>C	ENSP00000349685.2:p.Trp3302Ser
ENST00000358544.6:c.9980G>C	ENSP00000351346.2:p.Trp3327Ser
NM_017890.4:c.9980G>C , LRG_351t1:c.9980G>C	NP_060360.3:p.Trp3327Ser
NM_152564.4:c.9905G>C , LRG_351t2:c.9905G>C	NP_689777.3:p.Trp3302Ser
XM_005250800.2:c.9980G>C	XP_005250857.1:p.Trp3327Ser
XM_005250801.3:c.9980G>C	XP_005250858.1:p.Trp3327Ser
XM_011516848.1:c.9977G>C	XP_011515150.1:p.Trp3326Ser
XM_011516849.1:c.9902G>C	XP_011515151.1:p.Trp3301Ser
XM_011516850.1:c.9602G>C	XP_011515152.1:p.Trp3201Ser
XM_011516851.1:c.6866G>C	XP_011515153.1:p.Trp2289Ser
XM_011516852.1:c.6866G>C	XP_011515154.1:p.Trp2289Ser
XM_011516854.1:c.5759G>C	XP_011515156.1:p.Trp1920Ser
XM_005250800.3:c.9980G>C	XP_005250857.1:p.Trp3327Ser
XM_005250801.5:c.9980G>C	XP_005250858.1:p.Trp3327Ser
XM_011516848.2:c.9977G>C	XP_011515150.1:p.Trp3326Ser
XM_011516849.2:c.9902G>C	XP_011515151.1:p.Trp3301Ser
XM_011516850.2:c.9602G>C	XP_011515152.1:p.Trp3201Ser
XM_011516851.2:c.6866G>C	XP_011515153.1:p.Trp2289Ser
XM_011516852.2:c.6866G>C	XP_011515154.1:p.Trp2289Ser
XM_011516854.2:c.5759G>C	XP_011515156.1:p.Trp1920Ser
XM_017013109.1:c.9785G>C	XP_016868598.1:p.Trp3262Ser
XM_017013111.1:c.6866G>C	XP_016868600.1:p.Trp2289Ser
XM_017013112.1:c.5537G>C	XP_016868601.1:p.Trp1846Ser
XM_024447074.1:c.8765G>C	XP_024302842.1:p.Trp2922Ser
NM_017890.5:c.9980G>C MANE Plus Clinical	NP_060360.3:p.Trp3327Ser
NM_152564.5:c.9905G>C MANE Select	NP_689777.3:p.Trp3302Ser