Canonical Allele Identifier: CA371790688

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100874133G>C (hg19) ; chr8:g.99861905G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99861905G>C , CM000670.2:g.99861905G>C	GRCh38
NC_000008.10:g.100874133G>C , CM000670.1:g.100874133G>C	GRCh37
NC_000008.9:g.100943309G>C	NCBI36
NG_007098.2:g.853640G>C , LRG_351:g.853640G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.*343G>C	ENSP00000507923.1:n.*343G>C
ENST00000682358.1:n.11319G>C
ENST00000683334.1:c.*6931G>C	ENSP00000507369.1:n.*6931G>C
ENST00000357162.7:c.11174G>C MANE Select	ENSP00000349685.2:p.Gly3725Ala
ENST00000358544.7:c.11249G>C MANE Plus Clinical	ENSP00000351346.2:p.Gly3750Ala
ENST00000357162.6:c.11174G>C	ENSP00000349685.2:p.Gly3725Ala
ENST00000358544.6:c.11249G>C	ENSP00000351346.2:p.Gly3750Ala
NM_017890.4:c.11249G>C , LRG_351t1:c.11249G>C	NP_060360.3:p.Gly3750Ala
NM_152564.4:c.11174G>C , LRG_351t2:c.11174G>C	NP_689777.3:p.Gly3725Ala
XM_005250800.2:c.11249G>C	XP_005250857.1:p.Gly3750Ala
XM_005250801.3:c.11249G>C	XP_005250858.1:p.Gly3750Ala
XM_011516848.1:c.11246G>C	XP_011515150.1:p.Gly3749Ala
XM_011516849.1:c.11171G>C	XP_011515151.1:p.Gly3724Ala
XM_011516850.1:c.10871G>C	XP_011515152.1:p.Gly3624Ala
XM_011516851.1:c.8135G>C	XP_011515153.1:p.Gly2712Ala
XM_011516852.1:c.8135G>C	XP_011515154.1:p.Gly2712Ala
XM_011516854.1:c.7028G>C	XP_011515156.1:p.Gly2343Ala
XM_005250800.3:c.11249G>C	XP_005250857.1:p.Gly3750Ala
XM_005250801.5:c.11249G>C	XP_005250858.1:p.Gly3750Ala
XM_011516848.2:c.11246G>C	XP_011515150.1:p.Gly3749Ala
XM_011516849.2:c.11171G>C	XP_011515151.1:p.Gly3724Ala
XM_011516850.2:c.10871G>C	XP_011515152.1:p.Gly3624Ala
XM_011516851.2:c.8135G>C	XP_011515153.1:p.Gly2712Ala
XM_011516852.2:c.8135G>C	XP_011515154.1:p.Gly2712Ala
XM_011516854.2:c.7028G>C	XP_011515156.1:p.Gly2343Ala
XM_017013109.1:c.11054G>C	XP_016868598.1:p.Gly3685Ala
XM_017013111.1:c.8135G>C	XP_016868600.1:p.Gly2712Ala
XM_017013112.1:c.6806G>C	XP_016868601.1:p.Gly2269Ala
XM_024447074.1:c.10034G>C	XP_024302842.1:p.Gly3345Ala
NM_017890.5:c.11249G>C MANE Plus Clinical	NP_060360.3:p.Gly3750Ala
NM_152564.5:c.11174G>C MANE Select	NP_689777.3:p.Gly3725Ala