Canonical Allele Identifier: CA371790470
Gene: VPS13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.99861844G>C , CM000670.2:g.99861844G>C GRCh38
NC_000008.10:g.100874072G>C , CM000670.1:g.100874072G>C GRCh37
NC_000008.9:g.100943248G>C NCBI36
NG_007098.2:g.853579G>C , LRG_351:g.853579G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682153.1:c.*282G>C ENSP00000507923.1:n.*282G>C
ENST00000682358.1:n.11258G>C
ENST00000683334.1:c.*6870G>C ENSP00000507369.1:n.*6870G>C
ENST00000357162.7:c.11113G>C MANE Select ENSP00000349685.2:p.Glu3705Gln
ENST00000358544.7:c.11188G>C MANE Plus Clinical ENSP00000351346.2:p.Glu3730Gln
ENST00000357162.6:c.11113G>C ENSP00000349685.2:p.Glu3705Gln
ENST00000358544.6:c.11188G>C ENSP00000351346.2:p.Glu3730Gln
NM_017890.4:c.11188G>C , LRG_351t1:c.11188G>C NP_060360.3:p.Glu3730Gln
NM_152564.4:c.11113G>C , LRG_351t2:c.11113G>C NP_689777.3:p.Glu3705Gln
XM_005250800.2:c.11188G>C XP_005250857.1:p.Glu3730Gln
XM_005250801.3:c.11188G>C XP_005250858.1:p.Glu3730Gln
XM_011516848.1:c.11185G>C XP_011515150.1:p.Glu3729Gln
XM_011516849.1:c.11110G>C XP_011515151.1:p.Glu3704Gln
XM_011516850.1:c.10810G>C XP_011515152.1:p.Glu3604Gln
XM_011516851.1:c.8074G>C XP_011515153.1:p.Glu2692Gln
XM_011516852.1:c.8074G>C XP_011515154.1:p.Glu2692Gln
XM_011516854.1:c.6967G>C XP_011515156.1:p.Glu2323Gln
XM_005250800.3:c.11188G>C XP_005250857.1:p.Glu3730Gln
XM_005250801.5:c.11188G>C XP_005250858.1:p.Glu3730Gln
XM_011516848.2:c.11185G>C XP_011515150.1:p.Glu3729Gln
XM_011516849.2:c.11110G>C XP_011515151.1:p.Glu3704Gln
XM_011516850.2:c.10810G>C XP_011515152.1:p.Glu3604Gln
XM_011516851.2:c.8074G>C XP_011515153.1:p.Glu2692Gln
XM_011516852.2:c.8074G>C XP_011515154.1:p.Glu2692Gln
XM_011516854.2:c.6967G>C XP_011515156.1:p.Glu2323Gln
XM_017013109.1:c.10993G>C XP_016868598.1:p.Glu3665Gln
XM_017013111.1:c.8074G>C XP_016868600.1:p.Glu2692Gln
XM_017013112.1:c.6745G>C XP_016868601.1:p.Glu2249Gln
XM_024447074.1:c.9973G>C XP_024302842.1:p.Glu3325Gln
NM_017890.5:c.11188G>C MANE Plus Clinical NP_060360.3:p.Glu3730Gln
NM_152564.5:c.11113G>C MANE Select NP_689777.3:p.Glu3705Gln