Canonical Allele Identifier: CA462440279

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100729526T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99717298T>C , CM000670.2:g.99717298T>C	GRCh38
NC_000008.10:g.100729526T>C , CM000670.1:g.100729526T>C	GRCh37
NC_000008.9:g.100798702T>C	NCBI36
NG_007098.2:g.709033T>C , LRG_351:g.709033T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6657T>C	ENSP00000507923.1:p.Cys2219=
ENST00000682358.1:n.6727T>C
ENST00000683334.1:c.*2339T>C	ENSP00000507369.1:n.*2339T>C
ENST00000357162.7:c.6582T>C MANE Select	ENSP00000349685.2:p.Cys2194=
ENST00000358544.7:c.6657T>C MANE Plus Clinical	ENSP00000351346.2:p.Cys2219=
ENST00000357162.6:c.6582T>C	ENSP00000349685.2:p.Cys2194=
ENST00000358544.6:c.6657T>C	ENSP00000351346.2:p.Cys2219=
NM_017890.4:c.6657T>C , LRG_351t1:c.6657T>C	NP_060360.3:p.Cys2219=
NM_152564.4:c.6582T>C , LRG_351t2:c.6582T>C	NP_689777.3:p.Cys2194=
XM_005250800.2:c.6657T>C	XP_005250857.1:p.Cys2219=
XM_005250801.3:c.6657T>C	XP_005250858.1:p.Cys2219=
XM_011516848.1:c.6654T>C	XP_011515150.1:p.Cys2218=
XM_011516849.1:c.6579T>C	XP_011515151.1:p.Cys2193=
XM_011516850.1:c.6279T>C	XP_011515152.1:p.Cys2093=
XM_011516851.1:c.3543T>C	XP_011515153.1:p.Cys1181=
XM_011516852.1:c.3543T>C	XP_011515154.1:p.Cys1181=
XM_011516853.1:c.6657T>C	XP_011515155.1:p.Cys2219=
XM_011516854.1:c.2436T>C	XP_011515156.1:p.Cys812=
XM_005250800.3:c.6657T>C	XP_005250857.1:p.Cys2219=
XM_005250801.5:c.6657T>C	XP_005250858.1:p.Cys2219=
XM_011516848.2:c.6654T>C	XP_011515150.1:p.Cys2218=
XM_011516849.2:c.6579T>C	XP_011515151.1:p.Cys2193=
XM_011516850.2:c.6279T>C	XP_011515152.1:p.Cys2093=
XM_011516851.2:c.3543T>C	XP_011515153.1:p.Cys1181=
XM_011516852.2:c.3543T>C	XP_011515154.1:p.Cys1181=
XM_011516853.2:c.6657T>C	XP_011515155.1:p.Cys2219=
XM_011516854.2:c.2436T>C	XP_011515156.1:p.Cys812=
XM_017013109.1:c.6462T>C	XP_016868598.1:p.Cys2154=
XM_017013111.1:c.3543T>C	XP_016868600.1:p.Cys1181=
XM_017013112.1:c.2214T>C	XP_016868601.1:p.Cys738=
XM_024447074.1:c.5442T>C	XP_024302842.1:p.Cys1814=
NM_017890.5:c.6657T>C MANE Plus Clinical	NP_060360.3:p.Cys2219=
NM_152564.5:c.6582T>C MANE Select	NP_689777.3:p.Cys2194=