Canonical Allele Identifier: CA371776063

Gene: VPS13B

Linked Data

• MyVariant Identifiers: chr8:g.100831651A>C (hg19) ; chr8:g.99819423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99819423A>C , CM000670.2:g.99819423A>C	GRCh38
NC_000008.10:g.100831651A>C , CM000670.1:g.100831651A>C	GRCh37
NC_000008.9:g.100900827A>C	NCBI36
NG_007098.2:g.811158A>C , LRG_351:g.811158A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.8708A>C	ENSP00000507923.1:p.Asp2903Ala
ENST00000682358.1:n.8778A>C
ENST00000683334.1:c.*4390A>C	ENSP00000507369.1:n.*4390A>C
ENST00000357162.7:c.8633A>C MANE Select	ENSP00000349685.2:p.Asp2878Ala
ENST00000358544.7:c.8708A>C MANE Plus Clinical	ENSP00000351346.2:p.Asp2903Ala
ENST00000357162.6:c.8633A>C	ENSP00000349685.2:p.Asp2878Ala
ENST00000358544.6:c.8708A>C	ENSP00000351346.2:p.Asp2903Ala
NM_017890.4:c.8708A>C , LRG_351t1:c.8708A>C	NP_060360.3:p.Asp2903Ala
NM_152564.4:c.8633A>C , LRG_351t2:c.8633A>C	NP_689777.3:p.Asp2878Ala
XM_005250800.2:c.8708A>C	XP_005250857.1:p.Asp2903Ala
XM_005250801.3:c.8708A>C	XP_005250858.1:p.Asp2903Ala
XM_011516848.1:c.8705A>C	XP_011515150.1:p.Asp2902Ala
XM_011516849.1:c.8630A>C	XP_011515151.1:p.Asp2877Ala
XM_011516850.1:c.8330A>C	XP_011515152.1:p.Asp2777Ala
XM_011516851.1:c.5594A>C	XP_011515153.1:p.Asp1865Ala
XM_011516852.1:c.5594A>C	XP_011515154.1:p.Asp1865Ala
XM_011516854.1:c.4487A>C	XP_011515156.1:p.Asp1496Ala
XM_005250800.3:c.8708A>C	XP_005250857.1:p.Asp2903Ala
XM_005250801.5:c.8708A>C	XP_005250858.1:p.Asp2903Ala
XM_011516848.2:c.8705A>C	XP_011515150.1:p.Asp2902Ala
XM_011516849.2:c.8630A>C	XP_011515151.1:p.Asp2877Ala
XM_011516850.2:c.8330A>C	XP_011515152.1:p.Asp2777Ala
XM_011516851.2:c.5594A>C	XP_011515153.1:p.Asp1865Ala
XM_011516852.2:c.5594A>C	XP_011515154.1:p.Asp1865Ala
XM_011516854.2:c.4487A>C	XP_011515156.1:p.Asp1496Ala
XM_017013109.1:c.8513A>C	XP_016868598.1:p.Asp2838Ala
XM_017013111.1:c.5594A>C	XP_016868600.1:p.Asp1865Ala
XM_017013112.1:c.4265A>C	XP_016868601.1:p.Asp1422Ala
XM_024447074.1:c.7493A>C	XP_024302842.1:p.Asp2498Ala
NM_017890.5:c.8708A>C MANE Plus Clinical	NP_060360.3:p.Asp2903Ala
NM_152564.5:c.8633A>C MANE Select	NP_689777.3:p.Asp2878Ala